돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 128786생성일: 2026년 10월 24일

Sodium Hydroxide → (2E)-2-Methyl-7-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2-heptenol

https://huagongshe.com/ko/reaction/128786

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물Sodium hydrideHCID 24758—
반응물Triethyl 2-phosphonopropionateHCID 107155—
반응물Sodium BicarbonateHCID 516892—
반응물5-(2,6,6-Trimethyl-1-cyclohexen-1-yl)pentanalHCID 19375154—
반응물DiisobutylaluminumhydrideHCID 21225700—
용매TolueneHCID 1140—
용매TetrahydrofuranHCID 8028—
생성물(2E)-2-Methyl-7-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2-heptenolHCID 1937503543.1%

반응 단계

To a stirred solution of triethyl 2-phosphonopropionate (4.2 g) in THF (25 ml) under nitrogen is added sodium hydride (0.69 g of 60% dispersion in oil). After 30 minutes, 5-(2,6,6-trimethyl-1-cyclohexen-1-yl)pentanal (3.09 g) is added, and the mixture is stirred at reflux for16 hr. The reaction is cooled, poured into aqueous sodium bicarbonate, and extracted with ether. The extracts are concentrated and chromatographed with 30% dichloromethane in hexane to provide (2E)-2-methyl-7-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2-heptenoic add ethyl ester as a colorless oil (2.4 g). This material (2.09 g) is reacted with diisobutylaluminum hydride (10 ml of 1.5M toluene solution) in toluene (20 ml) at -20° , stirred at 0° for 3 hr, then stirred for 16 hr with 1.0N sodium hydroxide solution. The mixture is extracted with ether, and the organic phase is concentrated and chromatographed with dichloromethane to provide 1.6 g of (2E)-2-methyl-7-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2-heptenol as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05464865
출처 데이터셋uspto-grants-1995_11
ORD IDord-a201d8bc44424fc791242054bc5c15aa
출처 메모uspto-grants-1995_11