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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4505생성일: 2026년 10월 24일

1-Methylcyclohexanecarboxylic acid → 1-Cyclohexylethanol

https://huagongshe.com/ko/reaction/4505

반응식

참여 물질

역할이름HCID투입량
반응물1-Methylcyclohexanecarboxylic acidHCID 70744—
반응물Borane;tetrahydrofuranHCID 2723981—
용매TetrahydrofuranHCID 8028—
생성물1-CyclohexylethanolHCID 137829—

반응 조건

온도5 °C

반응 단계

A three liter, three necked round bottom flask was equipped with a thermometer, magnetic stirrer, argon inlet and outlet adapters and a one liter addition funnel containing 922 ml of 1.0 molar BH3.THF. 1-Methyl cyclohexanecarboxylic acid (119.2 g; 0.84 m) was added to the reaction vessel and dissolved in 100 ml of THF. The reaction mixture was cooled with an ice bath to 5° C. and the BH3.THF was added dropwise over 25 min maintaining the temperature between 5°-15° C. After the addition was complete, the ice bath was removed. After about five min, the reaction exothermed and foamed violently. A much slower addition rate and constant cooling should help to avoid this exotherm. The reaction was allowed to stir for two hr at RT under nitrogen, then 150 ml of methanol was added cautiously. When the foaming ceased, the reaction was concertrated in vacuo using low heat and the residue was treated with 100 ml of 5% acetic acid. After stirring for thirty min, the reaction was transferred to a one liter separatory funnel, diluted with water (slurry dissolved) and extracted three times with ether. The combined ether extracts were washed twice with saturated sodium bicarbonate, twice with brine, dried over anhydrous magnesium sulfate, filtered through celite and concentrated in vacuo (low heat) to give 79.09 g of a clear water-white oil. The oil was distilled on a Kugelrohr apparatus at 75°-130° C. (25 mm of Hg). Most distilled at 90° C. to give 72.11 g of 1-methyl-1-cyclohexylmethanol.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04727072
출처 데이터셋uspto-grants-1988_02
ORD IDord-dbacce31933a4d398510bac67d92c6e7
출처 메모uspto-grants-1988_02