돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 55406생성일: 2026년 10월 25일

Potassium Carbonate → (3aRS,7aRS)-2-benzyl-7,7-dimethyl-4-perhydroisoindolone

https://huagongshe.com/reaction/55406

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물2-Cyclohexen-1-one, 4,4-dimethyl-HCID 136839—
반응물N-Benzyl-1-butoxy-N-[(trimethylsilyl)methyl]methanamineHCID 11097910—
촉매Trifluoroacetic acidHCID 6422—
용매DichloromethaneHCID 6344—
생성물(3aRS,7aRS)-2-benzyl-7,7-dimethyl-4-perhydroisoindoloneHCID 67714335—

반응 단계

To a solution of 5 g of 4,4-dimethylcyclohex-2-enone and 12.4 cm3 of N-butoxymethyl-N-trimethylsilylmethylbenzylamine in 100 cm3 of dichloromethane are added, at a temperature of 10° C., 5 drops of trifluoroacetic acid. The reaction mixture is stirred at this temperature for 3 hours, then potassium carbonate is added and the solution is filtered through a sinter funnel and concentrated to dryness under reduced pressure (2.7 kPa). The residue is chromatographed on a column of silica gel (particle size 0.04-0.06 mm, diameter 5.2 cm, height 25 cm), eluting under a pressure of 0.5 bar of nitrogen with a mixture of cyclohexane and ethyl acetate (85/15 by volume) and collecting 100 cm3 fractions. Fractions 39 to 63 are combined and concentrated to dryness under reduced pressure (2.7 kPa). 3.64 g of (3aRS,7aRS)-2-benzyl-7,7-dimethyl-4-perhydroisoindolone are obtained in the form of a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05624950
출처 데이터셋uspto-grants-1997_04
ORD IDord-b19dfe6fd32d4b9786df94ca62e8fc2f
출처 메모uspto-grants-1997_04