反応 #4117177
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-0a8875fbd1ca4de39635404de98dbf99表示可能な構造データがありません
CCCC(CCC)CO製品情報
2-propylpentan-1-ol (CAS 58175-57-8) 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 123543
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
9 反応 · 9 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-0a8875fbd1ca4de39635404de98dbf99反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a mixture of 52 g 2-propylpentanol and 86 g of p-toluenesulfonic acid in 175 ml of chloroform was added at 0°-3° C. and under N2 -atmosphere 48 g of pyridine. The mixture was kept at 0° C. for 30 minutes and at room temperature for 19 hrs. After cooling the reaction mixture, 3M HCl (300 ml) was added. The organic phase was separated and washed with water and brine. Drying with Na2SO4 and evaporation gives 110 g of 2-propylpentyl tosylate. was added The organic phase was separated washed with water and brine Drying with Na2SO4 and evaporation
ソース ID: ord-8261f43ad94340078031a3efd1b300de反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a mixture of 52 g 2-propylpentanol and 86 g of p-toluenesulfonic acid in 175 ml of chloroform was added at 0°-3° C. and under N2 -atmosphere 48 g of pyridine. The mixture was kept at 0° C. for 30 minutes and at room temperature for 19 hrs. After cooling the reaction mixture, 3M HCl (300 ml) was added. The organic phase was separated and washed with water and brine. Drying with Na2SO4 and evaporation gives 110 g of 2-propylpentyl tosylate. was added The organic phase was separated washed with water and brine Drying with Na2SO4 and evaporation
ソース ID: ord-8261f43ad94340078031a3efd1b300de反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a mixture of 52 g 2-propylpentanol and 86 g of p-toluenesulfonic acid in 175 ml of chloroform was added at 0°-3° C. and under N2 -atmosphere 48 g of pyridine. The mixture was kept at 0° C. for 30 minutes and at room temperature for 19 hrs. After cooling the reaction mixture, 3M HCl (300 ml) was added. The organic phase was separated and washed with water and rine. Drying with Na2SO4 and evaporation gives 110 g of 2-propylpentyl tosylate. was added The organic phase was separated washed with water and rine Drying with Na2SO4 and evaporation
ソース ID: ord-cd54112771b740988c288c81990149ef反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a mixture of 52 g 2-propylpentanol and 86 g of p-toluenesulfonic acid in 175 ml of chloroform was added at 0°-3° C. and under N2 -atmosphere 48 g of pyridine. The mixture was kept at 0° C. for 30 minutes and at room temperature for 19 hrs. After cooling the reaction mixture, 3M HCl (300 ml) was added. The organic phase was separated and washed with water and brine. Drying with Na2SO4 and evaporation gives 110 g of 2-propylpentyl tosylate. was added The organic phase was separated washed with water and brine Drying with Na2SO4 and evaporation
ソース ID: ord-8261f43ad94340078031a3efd1b300de反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-0a8875fbd1ca4de39635404de98dbf99反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Phosphorus tribromide (33.3 g, 0.123 mol) was added dropwise to 2-propyl-1-pentanol (40 g, 0.307 mol) at −10° C. to maintain the temperature below 0° C. and the mixture was stirred overnight at room temperature. The reaction mixture was heated at 100° C. for 1 h, cooled to room temperature, and poured into ice water (250 ml). The organic layer was separated, washed with conc. H2SO4 (25 ml) followed by saturated K2CO3 (25 ml), dried and distilled in vacuo (80° C./15 mm Hg) to furnish 40 g (83%) of 1-bromo-2-propylpentane. to maintain the temperature below 0° C. The reaction mixture was heated at 100° C. for 1 h cooled to room temperature The organic layer was separated washed with conc. H2SO4 (25 ml) dried distilled in vacuo (80° C./15 mm Hg)
ソース ID: ord-65842f7768b24098bcd46cc7dc77358f反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a mixture of 52 g 2-propylpentanol and 86 g of p-toluenesulfonic acid in 175 ml of chloroform was added at 0°-3° C. and under N2 -atmosphere 48 g of pyridine. The mixture was kept at 0° C. for 30 minutes and at room temperature for 19 hrs. After cooling the reaction mixture, 3M HCl (300 ml) was added. The organic phase was separated and washed with water and rine. Drying with Na2SO4 and evaporation gives 110 g of 2-propylpentyl tosylate. was added The organic phase was separated washed with water and rine Drying with Na2SO4 and evaporation
ソース ID: ord-cd54112771b740988c288c81990149ef反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a mixture of 52 g 2-propylpentanol and 86 g of p-toluenesulfonic acid in 175 ml of chloroform was added at 0°-3° C. and under N2 -atmosphere 48 g of pyridine. The mixture was kept at 0° C. for 30 minutes and at room temperature for 19 hrs. After cooling the reaction mixture, 3M HCl (300 ml) was added. The organic phase was separated and washed with water and brine. Drying with Na2SO4 and evaporation gives 110 g of 2-propylpentyl tosylate. was added The organic phase was separated washed with water and brine Drying with Na2SO4 and evaporation
ソース ID: ord-8261f43ad94340078031a3efd1b300dePubChem 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。
