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HRID 55406作成日:2026年10月25日

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

https://huagongshe.com/reaction/55406

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物2-Cyclohexen-1-one, 4,4-dimethyl-HCID 136839—
反応物N-Benzyl-1-butoxy-N-[(trimethylsilyl)methyl]methanamineHCID 11097910—
触媒Trifluoroacetic acidHCID 6422—
溶媒DichloromethaneHCID 6344—
生成物(3aRS,7aRS)-2-benzyl-7,7-dimethyl-4-perhydroisoindoloneHCID 67714335—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05624950
出典データセットuspto-grants-1997_04
ORD IDord-b19dfe6fd32d4b9786df94ca62e8fc2f
出典メモuspto-grants-1997_04