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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 489915생성일: 2026년 10월 26일

Hydrochloric Acid → Methyl 1-benzylpyrrolidine-3-carboxylate

https://huagongshe.com/reaction/489915

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Methyl 1-benzyl-5-oxopyrrolidine-3-carboxylateHCID 98909—
반응물Borane;tetrahydrofuranHCID 2723981—
용매TetrahydrofuranHCID 8028—
생성물Methyl 1-benzylpyrrolidine-3-carboxylateHCID 46107513%

반응 단계

To a solution of 1-benzyl-5-oxo-pyrrolidine-3-carboxylic acid methyl ester (30 mmol, 7 g) in anhydrous tetrahydrofuran (40 ml) was added borane-tetrahydrofuran solution (1M, 50 mmol, 50 mL) at ambient temperature. When gas evolution had subsided the solution was heated under reflux for 75 min then stirred for 16 hr at ambient temperature. Hydrochloric acid (6M) was added dropwise (ca. 5 mL) and the mixture was stirred at ambient temperature for 1 hr before removing the solvent under vacuum. The residue was dissolved in dichloromethane and the solution was washed with dilute sodium hydroxide solution. The dichloromethane solution was then extracted with dilute hydrochloric acid (×3), the extracts combined, made basic by addition of sodium hydroxide and extracted with dichloromethane (×3). The combined organic extract was dried over anhydrous sodium sulfate and the solvent was removed under vacuum. The product was purified by chromatography on silica gel eluting with 5% methanol-dichloromethane to give 1-benzyl-pyrrolidine-3-carboxylic acid methyl ester (200 mg, 3%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06979741B2
출처 데이터셋uspto-grants-2005_12
ORD IDord-03eb48fd686e4482bb584f621892f2eb
출처 메모uspto-grants-2005_12