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HRID 1028935作成日:2026年10月27日

Pyrrolidine → 1-(2-Bromo-3-methylbenzoyl)pyrrolidine

https://huagongshe.com/reaction/1028935

反応式

関与物質

役割名称HCID仕込み量
反応物PyrrolidineHCID 31268—
反応物2-Bromo-3-methylbenzoic acidHCID 2735588—
溶媒TetrahydrofuranHCID 8028—
生成物1-(2-Bromo-3-methylbenzoyl)pyrrolidineHCID 66579149—

反応手順

2-Bromo-3-methylbenzoic acid (5.0 g, 23.3 mmol) was dissolved in THF (100 mL) and added N,N′-carbonyldiimidazole (4.52 g, 27.9 mmol). The reaction mixture was stirred at ambient temperature for 14 h. Pyrrolidine (6.8 mL, 81 mmol) was added in one portion. The mixture was stirred for 8 h and then partitioned between EtOAc and water. The organic layer was washed with water, diluted HCl, saturated bicarbonate, water and brine. The solution was then concentrated in vacuo to afford (2-bromo-3-methylphenyl)(pyrrolidin-1-yl)methanone as a white crystalline solid, upon standing overnight at RT.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08735384B2
出典データセットuspto-grants-2014_05
ORD IDord-a11937687535417686898b6081575465
出典メモuspto-grants-2014_05