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HRID 1028935생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1028935

반응식

참여 물질

역할이름HCID투입량
반응물PyrrolidineHCID 31268—
반응물2-Bromo-3-methylbenzoic acidHCID 2735588—
용매TetrahydrofuranHCID 8028—
생성물1-(2-Bromo-3-methylbenzoyl)pyrrolidineHCID 66579149—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08735384B2
출처 데이터셋uspto-grants-2014_05
ORD IDord-a11937687535417686898b6081575465
출처 메모uspto-grants-2014_05