反応 #4018853
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-c8002afb3b06404584f6de3e7f4af8aa表示可能な構造データがありません
CCCCCCC(=O)CCC(=O)OC製品情報
methyl 4-oxodecanoate (CAS 7011-82-7) 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 538627
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
5 反応 · 5 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-c8002afb3b06404584f6de3e7f4af8aa反応条件: temp:25.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To the resulting isobutyl 4-oxodecanoate were added 1 L of methanol and 250 g of 25% sodium hydroxide, and the mixture was stirred at 25° C. for 1 hour, followed by distilling off methanol in vacuo. Subsequently, thereto were added 2 L of water and 1 L of toluene. The resulting mixture was stirred at room temperature for 1 hour and then allowed to stand to separate the water phase. To the water phase were added 175 g of concentrated hydrochloric acid and 1.8 L of toluene. The resulting mixture was stirred for 10 minutes and then allowed to stand to separate the organic phase. Toluene in the organic phase was distilled off in vacuo and 1 L of toluene and 47.5 mL of concentrated sulfuric acid were added. The resulting mixture was heated under reflux for 1 hour and then cooled to 25° C. Thereto was gradually added 155 g of sodium hydrogencarbonate followed by stirring for 10 minutes at 25° C. Methanol was distilled off in vacuo and then 3 L of water and 1.8 L of toluene were added. The resulting mixture was stirred for 10 minutes at room temperature and then allowed to stand to separate the organic phase. Toluene in the organic phase was distilled off, yielding methyl 4-oxodecanoate (a compound in which R17 represents an n-pentyl group, and R18 represents a methyl group in the above formula (12)). Gas chromatographic analysis showed that the yield of methyl 4-oxodecanoate relative to isobutyl 4-oxodecanoate was 95%. by distilling off methanol in vacuo Subsequently, thereto were added 2 L of water and 1 L of toluene The resulting mixture was stirred at room temperature for 1 hour to separate the water phase To the water phase were added 175 g of concentrated hydrochloric acid and 1.8 L of toluene The resulting mixture was stirred for 10 minutes to separate the organic phase Toluene in the organic phase was distilled off in vacuo and 1 L of toluene and 47.5 mL of concentrated sulfuric acid were added The resulting mixture was heated under reflux for 1 hour cooled to 25° C by stirring for 10 minutes at 25° C Methanol was distilled off in vacuo 3 L of water and 1.8 L of toluene were added The resulting mixture was stirred for 10 minutes at room temperature to separate the organic phase Toluene in the organic phase was distilled off
ソース ID: ord-0535824467e640658d22b42a72a705c0反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-c8002afb3b06404584f6de3e7f4af8aa反応条件: temp:25.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To the resulting isobutyl 4-oxodecanoate were added 1 L of methanol and 250 g of 25% sodium hydroxide, and the mixture was stirred at 25° C. for 1 hour, followed by distilling off methanol in vacuo. Subsequently, thereto were added 2 L of water and 1 L of toluene. The resulting mixture was stirred at room temperature for 1 hour and then allowed to stand to separate the water phase. To the water phase were added 175 g of concentrated hydrochloric acid and 1.8 L of toluene. The resulting mixture was stirred for 10 minutes and then allowed to stand to separate the organic phase. Toluene in the organic phase was distilled off in vacuo and 1 L of toluene and 47.5 mL of concentrated sulfuric acid were added. The resulting mixture was heated under reflux for 1 hour and then cooled to 25° C. Thereto was gradually added 155 g of sodium hydrogencarbonate followed by stirring for 10 minutes at 25° C. Methanol was distilled off in vacuo and then 3 L of water and 1.8 L of toluene were added. The resulting mixture was stirred for 10 minutes at room temperature and then allowed to stand to separate the organic phase. Toluene in the organic phase was distilled off, yielding methyl 4-oxodecanoate (a compound in which R17 represents an n-pentyl group, and R18 represents a methyl group in the above formula (12)). Gas chromatographic analysis showed that the yield of methyl 4-oxodecanoate relative to isobutyl 4-oxodecanoate was 95%. by distilling off methanol in vacuo Subsequently, thereto were added 2 L of water and 1 L of toluene The resulting mixture was stirred at room temperature for 1 hour to separate the water phase To the water phase were added 175 g of concentrated hydrochloric acid and 1.8 L of toluene The resulting mixture was stirred for 10 minutes to separate the organic phase Toluene in the organic phase was distilled off in vacuo and 1 L of toluene and 47.5 mL of concentrated sulfuric acid were added The resulting mixture was heated under reflux for 1 hour cooled to 25° C by stirring for 10 minutes at 25° C Methanol was distilled off in vacuo 3 L of water and 1.8 L of toluene were added The resulting mixture was stirred for 10 minutes at room temperature to separate the organic phase Toluene in the organic phase was distilled off
ソース ID: ord-0535824467e640658d22b42a72a705c0反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-c8002afb3b06404584f6de3e7f4af8aaPubChem 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。
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