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HRID 654519作成日:2026年10月25日

Methyl 1-benzyl-5-oxopyrrolidine-3-carboxylate → Methyl 1-benzylpyrrolidine-3-carboxylate

https://huagongshe.com/reaction/654519

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 1-benzyl-5-oxopyrrolidine-3-carboxylateHCID 98909—
反応物Borane;tetrahydrofuranHCID 2723981—
反応物Hydrochloride methanolHCID 21893726—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 1-benzylpyrrolidine-3-carboxylateHCID 461075150.2%

反応手順

A solution of methyl 1-benzyl-2-oxo-4-pyrrolidylcarboxylate (D10, 35.4 g, 0.18 mole) in dry THF (135 ml) was added dropwise over 30 mins to 1M borane-THF solution (228 ml, 0.23 mole) at 0° C. under nitrogen, and when addition was complete the solution was heated under reflux for 1h. The solution was cooled to room temperature, then treated dropwise with 8% hydrogen chloride/methanol (114 ml, 0.25 mole HCl) and stirred for 18h, followed by 3h at reflux. The mixture was then concentrated in vacuo and the residue treated with water (40 ml), washed with ether (2×50 ml), basified with 40% sodium hydroxide solution, saturated with potassium carbonate and extracted with ether (3×70 ml). The combined extracts were dried (Na2SO4) and concentrated in vacuo to leave a yellow oil, which was purified by distillation (b.p. 146° C.0.7mm) to give the title compound (D11) as a colourless oil (19.8 g, 50%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05132316
出典データセットuspto-grants-1992_07
ORD IDord-d7fce74ab2f8417f9631c77014014c0e
出典メモuspto-grants-1992_07