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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 132980생성일: 2026년 10월 25일

Isobutylene oxide → 2-[1-(3,3-Dimethyl-cyclohexyl)-ethoxy]-2-methyl-propan-1-ol

https://huagongshe.com/reaction/132980

반응식

참여 물질

역할이름HCID투입량
반응물Isobutylene oxideHCID 11208—
반응물Cyclohexanemethanol, alpha,3,3-trimethyl-HCID 91338—
반응물Ethyl aluminium dichlorideHCID 16686341—
용매TolueneHCID 1140—
용매CyclohexaneHCID 8078—
생성물2-[1-(3,3-Dimethyl-cyclohexyl)-ethoxy]-2-methyl-propan-1-olHCID 1202201238%

반응 단계

At 0° C. under an atmosphere of nitrogen, 178 ml (321 mmol) of a 1.8 M solution of ethyl aluminium dichloride in toluene was slowly added to a stirred solution of 100 g (641 mmol) of 1-(3′,3′-dimethylcyclohexyl)ethanol and 55.4 g (769 mmol) of isobutylenoxide in 500 ml of cyclohexane. After complete addition, the cooling bath was removed, the reaction mixture was allowed to warm to room temperature, and stirring was continued at this temperature for 15 h. The reaction mixture was then poured into 1 L of brine, acidified with concentrated phosphoric acid, and thrice extracted with ether. The combined organic extracts were washed with brine and water, dried with sodium sulphate, and concentrated on a rotary evaporator. Distillation of the crude material (136 g) provided at 78-85° C./0.3 mbar 55.1 g (38%) of pure 2-[1′-(3″,3″-dimethylcyclohexyl)-ethoxy]-2-methylpropan-1-ol, while 60.4 g of starting material were recovered.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07390779B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-c2a06d032eff4e9d975790186acbc953
출처 메모uspto-grants-2008_06