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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1764170생성일: 2026년 10월 26일

Methanesulfonic Acid → 3,5,5-Trimethyl-3-(t-butylperoxy) cyclohexanol

https://huagongshe.com/reaction/1764170

반응식

참여 물질

역할이름HCID투입량
반응물Methanesulfonic AcidHCID 6395—
반응물3,5,5-TRIMETHYL-3-(t-BUTYLPEROXY)CYCLOHEXANONEHCID 20570473—
반응물HCID 178418361HCID 178418361—
촉매PlatinumHCID 23939—
용매Diethyl EtherHCID 3283—
생성물3,5,5-Trimethyl-3-(t-butylperoxy) cyclohexanolHCID 20306798—

반응 단계

The catalytic hydrogenation of 3,5,5-trimethyl-3-(t-butylperoxy)-cyclohexanone, 10.0 g. (0.045 mole), was carried out in a Parr Hydrogenation Apparatus using 1.0 g. 5% Platinum on carbon catalyst and in the presence of 50 ml. of 10% methanesulfonic acid solution. The hydrogenation at 60 p.s.i.g. hydrogen pressure was started at 0° C. and the temperature allowed to rise to 21° C. After 2 1/2 hours, the reaction was stopped, the product taken up in ether, the etheral solution washed to neutrality with water, dried over anhydrous magnesium sulfate and the ether removed under reduced pressure. Examination of the IR spectrum of the product showed that some of the desired product had been obtained as evidenced by the hydroxyl absorption band while some unreduced carbonyl was still present. Further catalytic hydrogenation at 35° C. for 18 hours caused a further increase in hydroxyl absorption band and reduction of the carbonyl absorption band.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04115455
출처 데이터셋uspto-grants-1978_09
ORD IDord-36143b888cef4e3a95fe33787ddc8c89
출처 메모uspto-grants-1978_09