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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 42729생성일: 2026년 10월 25일

Pyridine → 1-(2,2,4-trimethyl-cyclohex-3-enyl)-ethanone O-methyl-oxime

https://huagongshe.com/reaction/42729

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물O-Methylhydroxylamine hydrochlorideHCID 521874—
반응물1-(2,2,4-Trimethyl-3-cyclohexen-1-yl)ethan-1-oneHCID 3016988—
용매MethanolHCID 887—
생성물1-(2,2,4-trimethyl-cyclohex-3-enyl)-ethanone O-methyl-oximeHCID 8667533892.4%

반응 조건

온도24 °C

반응 단계

To a stirred solution of 1-(2,2,4-trimethyl-cyclohex-3-enyl)-ethanone (162 g; 0.97 mol), prepared as described in example P4, in methanol (500 ml) was added pyridine (160 ml; 1.95 mol) followed by a portionwise addition of methoxyamine hydrochloride (142 g; 1.70 mol). The reaction mixture was stirred at 24° C. for 16 hours under nitrogen atmosphere. Methanol was removed under reduced pressure, the residue poured in water (600 ml) and 1N hydrochloric acid was added (100 ml). The solution was extracted with dichloromethane (3×300 ml). Combined organic layers were washed with brine (500 ml) and dried over sodium sulfate. The solvent was removed in vacuo to afford 175 g (92% of theory) of 1-(2,2,4-trimethyl-cyclohex-3-enyl)-ethanone O-methyl-oxime as a clear red oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536215B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-949bef1b62f54a69bbcb37a365ea0c46
출처 메모uspto-grants-2013_09