참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 2-Cyclohexen-1-one, 4,4-dimethyl- | HCID 136839 | — |
| 반응물 | N-Benzyl-1-butoxy-N-[(trimethylsilyl)methyl]methanamine | HCID 11097910 | — |
| 촉매 | Trifluoroacetic acid | HCID 6422 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (3aRS,7aRS)-2-benzyl-7,7-dimethyl-4-perhydroisoindolone | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US05624950 |
|---|
| 출처 데이터셋 | uspto-grants-1997_04 |
|---|
| ORD ID | ord-b19dfe6fd32d4b9786df94ca62e8fc2f |
|---|
| 출처 메모 | uspto-grants-1997_04 |
|---|