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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 223606생성일: 2026년 10월 24일

Ammonia → 2,3,6-Trimethylcyclohexan-1-one

https://huagongshe.com/ko/reaction/223606

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물4-MethylmorpholineHCID 7972—
반응물2-Cyclohexen-1-one, 2,5,6-trimethyl-HCID 89264—
촉매PalladiumHCID 23938—
촉매ZincHCID 23994—
생성물2,3,6-Trimethylcyclohexan-1-oneHCID 142583—
생성물2,3,6-TrimethylanilineHCID 11958947—

반응 단계

In a stirred autoclave having a useful capacity of 300 parts by volume, a solution of 35 parts of 2,3,6-trimethylcyclohex-5-en-1-one in 35 parts of N-methylmorpholine, 34 parts of ammonia and 5 parts of a finely divided catalyst, containing 0.5% by weight of Pd and 0.1% by weight of Zn on Al2O3, are kept for 10 hours at 230° C. and the autogenous pressure (about 150 bar). The mixture is then allowed to cool, filtered and purified by distillation. 18.2 parts of 2,3,6-trimethylaniline and 15.3 parts of 2,3,6-trimethylcyclohexan-1-one are obtained, the latter presumably through partial hydrogenation of the 2,3,6-trimethylcyclohex-5-en-1-one starting material with the hydrogen formed during the reaction. Since 2,3,6-trimethylcyclohexan-1-one can in turn be converted to the desired 2,3,6-trimethylaniline, for example as described in Example 1 or 2, the selectivity of the reaction is 96%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04355180
출처 데이터셋uspto-grants-1982_10
ORD IDord-7a776762b5914e1cb244a050d0a88372
출처 메모uspto-grants-1982_10