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HRID 1374075생성일: 2026년 10월 25일

Triethylamine → (3-Bromo-2-oxo-pyrrolidin-1-yl)benzoic acid benzyl ester

https://huagongshe.com/reaction/1374075

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Sodium HydroxideHCID 14798—
반응물Benzyl p-aminobenzoateHCID 98488—
반응물2,4-Dibromobutyryl chlorideHCID 4413143—
반응물1-Butanaminium, N,N,N-tributyl-, carbonic acid (1:1)HCID 11012140—
용매DichloromethaneHCID 6344—
생성물(3-Bromo-2-oxo-pyrrolidin-1-yl)benzoic acid benzyl esterHCID 69484365—

반응 단계

45.5 g (0.2 mol) of 4-aminobenzoic acid benzyl ester and 30.6 ml (0.22 mol) of triethylamine are dissolved in 200 ml of methylene chloride and added in drops at 0° C. to a solution of 52.9 g (0.2 mol) of 2,4-dibromobutyric acid chloride (Gramin et al. Synth. Commun. (1997), (27), 1827) in 200 ml of methylene chloride within 45 minutes, and it is stirred for 18 hours at room temperature. The reaction mixture is now added in drops at 0° C. to a solution of 400 ml of aqueous 32% sodium hydroxide and 2 g of tetrabutylammonium hydrogen carbonate (about 15 minutes), and it is stirred for 30 minutes. Then, the phases are separated, and the aqueous phase is extracted three times with 200 ml of dichloromethane each. The organic phases are dried on sodium sulfate, the solution is evaporated to the dry state and chromatographed on silica gel (methylene chloride). The fractions that contain the product are combined and concentrated by evaporation.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07164016B2
출처 데이터셋uspto-grants-2007_01
ORD IDord-72bb3e4e60cc414a964cc1fb33f65dc1
출처 메모uspto-grants-2007_01