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HRID 354274作成日:2026年10月26日

tert-Butyl 2-(2,2-dibromoethenyl)pyrrolidine-1-carboxylate → tert-Butyl 2-ethynylpyrrolidine-1-carboxylate

https://huagongshe.com/reaction/354274

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butyl 2-(2,2-dibromoethenyl)pyrrolidine-1-carboxylateHCID 14730280—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物tert-Butyl 2-ethynylpyrrolidine-1-carboxylateHCID 1473028397%

反応手順

To a stirred cold (minus 78° C.) solution of 1-(tert-butoxycarbonyl)-2-(2,2-dibromoethenyl)pyrrolidine (7.81 g, 22 mmol) in THF (200 mL) was added n-BuLi (1.59 M in hexane, 28 mL, 44 mmol) over 10 min. and the stirring was continued for 2 hr at the same temp. The reaction was quenched by the addition of sat. NH4Cl and extracted with EtOAc. The extract was washed with brine, dried over MgSO4, and evaporated. The residue was chromatographed on silica-gel with n-hexane-AcOEt (10:1, v/v) as eluent to give 4.15 g (97%) 1-(tert-butoxycarbonyl)-2-ethynyl pyrrolidine as a light yellow oil. 1H-NMR (CDCl3) δ1.48 (9 H, s), 1.82-2.21 (4 H, m), 3.30-3.45 (2 H, m), 4.41-4.52 (1 H, m).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06756378B2
出典データセットuspto-grants-2004_06
ORD IDord-6076674b8c2e46b9bd8735b53ecc9621
出典メモuspto-grants-2004_06