反応 #3878439
関連文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-48bc8f1e254c47359b985b3adb0a807e表示可能な構造データがありません
CCCCCCCC1CCC(=O)O1製品情報
5-heptyloxolan-2-one (CAS 104-67-6) product identity, structure identifiers and related reaction data for chemical intermediate research and sourcing review.
想定用途
専門的研究・工業用途限定
データベース ID 7714
安全上の注意
For professional research and industrial use only. Review the supplier safety data sheet before handling.
合成データ
12 反応 · 12 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-48bc8f1e254c47359b985b3adb0a807e反応条件: temp:65.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a mixture of 203 g 5-heptyl-dihydro-furan-2-one and 390 g dimethylcarbonate was slowly added 40 g of sodium hydride. The temperature increased to 65° C. After the temperature returned to room temperature, the reaction mixture was poured into saturated citric acid and extracted with hexane. The organic layer was dried and evaporated to dryness. The residue was distilled to yield 150.5 g of a colourless liquid. returned to room temperature extracted with hexane The organic layer was dried evaporated to dryness The residue was distilled
ソース ID: ord-ae3aad03df2e4781a7b3f3048e48aac5反応条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A solution of 19.0 g aluminum chloride, dissolved in methylene chloride, was cooled to 0° C. and 46.5 g dodecylamine in methylene chloride was added dropwise (exothermic). At room temperature 19.3 g gamma-undecalactone was added rapidly. The temperature rose to 36° C. The reaction was stirred at room temperature for 4 hours. The mixture was quenched with water and filtered over Celite. The liquid was extracted with ether and washed with water and brine. The solution was dried, filtered and evaporated to dryness. The resulting brown crystals were purified by recrystallization from ether/ethylacetate to give pale yellow crystals. rose to 36° C The mixture was quenched with water filtered over Celite The liquid was extracted with ether washed with water and brine The solution was dried filtered evaporated to dryness The resulting brown crystals were purified by recrystallization from ether/ethylacetate to give pale yellow crystals
ソース ID: ord-36b6ad299faa48fcaa5d705b6b120e80反応条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A solution of 19.0 g aluminum chloride, dissolved in methylene chloride, was cooled to 0° C. and 46.5 g dodecylamine in methylene chloride was added dropwise (exothermic). At room temperature 19.3 g gamma-undecalactone was added rapidly. The temperature rose to 36° C. The reaction was stirred at room temperature for 4 hours. The mixture was quenched with water and filtered over Celite. The liquid was extracted with ether and washed with water and brine. The solution was dried, filtered and evaporated to dryness. The resulting brown crystals were purified by recrystallization from ether/ethylacetate to give pale yellow crystals. rose to 36° C The mixture was quenched with water filtered over Celite The liquid was extracted with ether washed with water and brine The solution was dried filtered evaporated to dryness The resulting brown crystals were purified by recrystallization from ether/ethylacetate to give pale yellow crystals
ソース ID: ord-36b6ad299faa48fcaa5d705b6b120e80反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a solution of 43.6 g sodium hydroxide in 150 ml of methanol heated to reflux, 200 g gamma-undecalactone were added. After stirring for 2 hours at reflux, the mixture was cooled to room temperature and evaporated to dryness. The resulting crystals were washed with hexane to yield 240 g of colorless crystals. to reflux at reflux evaporated to dryness The resulting crystals were washed with hexane
ソース ID: ord-bd3b95f7201f438a9fc4ec872a72edcd反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a suspension of 19.0 g aluminum trichloride in 50 ml of dichloromethane, a solution of 46.5 g dodecylamine in 50 ml of dichloromethane was dropped in at 15-20° C. Then 19.3 g gamma-undecalactone were added quickly at room temperature and an additional 50 ml of dichloromethane was added. After 4 hours, the reaction mixture was quenched with water and filtered through celite. The filtrate was diluted with ether and washed with brine. The organic phase was dried, filtered and evaporated to dryness. The resulting brown solid was purified by recrystallisation to yield 2.65 g of colourless crystals. the reaction mixture was quenched with water filtered through celite The filtrate was diluted with ether washed with brine The organic phase was dried filtered evaporated to dryness The resulting brown solid was purified by recrystallisation
ソース ID: ord-15f10c7439844911ab977e3fa5c6c16f反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a suspension of 19.0 g aluminum trichloride in 50 ml of dichloromethane, a solution of 46.5 g dodecylamine in 50 ml of dichloromethane was dropped in at 15-20° C. Then 19.3 g gamma-undecalactone were added quickly at room temperature and an additional 50 ml of dichloromethane was added. After 4 hours, the reaction mixture was quenched with water and filtered through celite. The filtrate was diluted with ether and washed with brine. The organic phase was dried, filtered and evaporated to dryness. The resulting brown solid was purified by recrystallisation to yield 2.65 g of colourless crystals. the reaction mixture was quenched with water filtered through celite The filtrate was diluted with ether washed with brine The organic phase was dried filtered evaporated to dryness The resulting brown solid was purified by recrystallisation
ソース ID: ord-15f10c7439844911ab977e3fa5c6c16f反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a solution of 43.6 g sodium hydroxide in 150 ml of methanol heated to reflux, 200 g gamma-undecalactone were dropped in. After stirring 2 hours at reflux, the mixture was cooled to room temperature and evaporated to dryness. The resulting crystals were washed with hexane to yield 240 g white crystals. to reflux at reflux evaporated to dryness The resulting crystals were washed with hexane
ソース ID: ord-8b7e64279c8f4644896391501f3eeae2反応条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A solution of 19.0 g aluminum chloride, dissolved in methylene chloride, was cooled to 0° C. and 46.5 g dodecylamine in methylene chloride was added dropwise (exothermic). At room temperature, 19.3 g gamma-undecalactone was added rapidly. The temperature rose to 36° C. The reaction was stirred at room temperature for 4 hours. The mixture was quenched with water and filtered over Celite. The liquid was extracted with ether and washed with water and brine. The solution was dried, filtered and evaporated to dryness. The resulting brown crystals were purified by recrystallization from ether/ethylacetate to give pale yellow crystals. rose to 36° C The mixture was quenched with water filtered over Celite The liquid was extracted with ether washed with water and brine The solution was dried filtered evaporated to dryness The resulting brown crystals were purified by recrystallization from ether/ethylacetate to give pale yellow crystals
ソース ID: ord-491a19afb3174b878e9a949db83ba780反応条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A solution of 19.0 g aluminum chloride, dissolved in methylene chloride, was cooled to 0° C. and 46.5 g dodecylamine in methylene chloride was added dropwise (exothermic). At room temperature, 19.3 g gamma-undecalactone was added rapidly. The temperature rose to 36° C. The reaction was stirred at room temperature for 4 hours. The mixture was quenched with water and filtered over Celite. The liquid was extracted with ether and washed with water and brine. The solution was dried, filtered and evaporated to dryness. The resulting brown crystals were purified by recrystallization from ether/ethylacetate to give pale yellow crystals. rose to 36° C The mixture was quenched with water filtered over Celite The liquid was extracted with ether washed with water and brine The solution was dried filtered evaporated to dryness The resulting brown crystals were purified by recrystallization from ether/ethylacetate to give pale yellow crystals
ソース ID: ord-491a19afb3174b878e9a949db83ba780反応条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A solution of 19.0 g aluminum chloride, dissolved in methylene chloride, was cooled to 0° C. and 46.5 g dodecylamine in methylene chloride was added dropwise (exothermic). At room temperature, 19.3 g gamma-undecalactone was added rapidly. The temperature rose to 36° C. The reaction was stirred at room temperature for 4 hours. The mixture was quenched with water and filtered over Celite. The liquid was extracted with ether and washed with water and brine. The solution was dried, filtered and evaporated to dryness. The resulting brown crystals were purified by recrystallization from ether/ethylacetate to give pale yellow crystals. rose to 36° C The mixture was quenched with water filtered over Celite The liquid was extracted with ether washed with water and brine The solution was dried filtered evaporated to dryness The resulting brown crystals were purified by recrystallization from ether/ethylacetate to give pale yellow crystals
ソース ID: ord-491a19afb3174b878e9a949db83ba780反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a solution of 43.6 g sodium hydroxide in 150 ml of methanol heated to reflux, 200 g gamma-undecalactone were added. After stirring for 2 hours at reflux, the mixture was cooled to room temperature and evaporated to dryness. The resulting crystals were washed with hexane to yield 240 g of colorless crystals. to reflux at reflux evaporated to dryness The resulting crystals were washed with hexane
ソース ID: ord-6594d88a1a1e47ee82c6308a03e457cePubChem References
化合物の公開データベース記録に掲載された情報源です。
関連製品
12 related records
CAS 32780-06-6
CAS 502-26-1
CAS 6938-94-9
CAS 10374-51-3
CAS 3123-97-5
CAS 2244716-48-9
CAS 32818-35-2
CAS 10233-13-3
CAS 110-27-0
CAS 62668-35-3
CAS 3301-94-8
CAS 3301-90-4
