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HRID 1917330作成日:2026年10月27日

Trifluoroacetic acid → rel-(3aR,6aR)-Methyl 2-benzylhexahydrocyclopenta[c]pyrrole-3a(1H)-carboxylate

https://huagongshe.com/reaction/1917330

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic acidHCID 6422—
反応物Benzyl(methoxymethyl)((trimethylsilyl)methyl)amineHCID 353442—
反応物Methyl cyclopent-1-ene-1-carboxylateHCID 549129—
溶媒DichloromethaneHCID 6344—
生成物rel-(3aR,6aR)-Methyl 2-benzylhexahydrocyclopenta[c]pyrrole-3a(1H)-carboxylateHCID 151551483%

反応手順

A catalytic amount of trifluoroacetic acid was added to a solution of 1-cyclopentene-1-carboxylic acid methyl ester (2.52 g, 20.0 mmol) and N-benzyl-N-(methoxymethyl)-N-trimethylsilylmethylamine (5.00 g, 21.1 mmol) in dichloromethane (40 mL) at room temperature, and the mixture was heated with stirring at room temperature for 15.5 hours. The reaction solution was diluted with dichloromethane (100 mL) and washed with a saturated sodium bicarbonate solution (80 mL). The washed aqueous layer was further extracted with dichloromethane (50 mL). The organic layers were combined and dried over anhydrous sodium sulfate. After filtration, the solvent was evaporated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=95:5→90:10→80:20) to give 4.28 g (83%) of the title compound as a colorless transparent oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08618094B2
出典データセットuspto-grants-2013_12
ORD IDord-0be8207185c648c4ab86050b9ee72355
出典メモuspto-grants-2013_12