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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 484570생성일: 2026년 10월 25일

2-Heptanol, 6-methyl- → 6-Methyl-2-heptanone

https://huagongshe.com/reaction/484570

반응식

참여 물질

역할이름HCID투입량
반응물2-Heptanol, 6-methyl-HCID 96476—
반응물HCID 178418287HCID 178418287—
용매Diethyl EtherHCID 3283—
용매DichloromethaneHCID 6344—
용매Sodium HydroxideHCID 14798—
생성물6-Methyl-2-heptanoneHCID 1357297%

반응 단계

A mixture of 1.27 g (9.76 mmoles) of 6-methyl-2-heptanol (purchased from Aldrich Chemical Co., Milwaukee, Wis.) and 9.26 g (42.9 mmoles) of pyridinium chlorochromate (purchased from Aldrich Chemical Co., Milwaukee, Wis.) in 35 mL of dichloromethane was stirred at room temperature for 3.5 hours. At that point, the mixture was diluted with 150 mL of ether and 200 mL of 1M aqueous sodium hydroxide. After separating the layers, the organic layer was washed in successive order with 9:1 (volume/volume) 1M aqueous sodium hydroxide: saturated brine (2×100 mL), 10% aqueous sodium chloride (1×100 mL), 3:1 (volume/volume) 2M aqueous hydrochloric acid: saturated brine (3×100 mL), saturated aqueous sodium bicarbonate (1×100 mL), and saturated brine (1×100 mL). The organic layer was then dried over anhydrous magnesium sulfate and filtered. Removal of the volatile organic solvents by evaporation at reduced pressure afforded 1.214 g (97% yield) of the named ketone. The identity and purity of this known compound were ascertained by IR and proton NMR analysis.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05231232
출처 데이터셋uspto-grants-1993_07
ORD IDord-f45e267723ad401e85fca862ef5308da
출처 메모uspto-grants-1993_07