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HRID 1374075作成日:2026年10月26日

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

https://huagongshe.com/reaction/1374075

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Sodium HydroxideHCID 14798—
反応物Benzyl p-aminobenzoateHCID 98488—
反応物2,4-Dibromobutyryl chlorideHCID 4413143—
反応物1-Butanaminium, N,N,N-tributyl-, carbonic acid (1:1)HCID 11012140—
溶媒DichloromethaneHCID 6344—
生成物(3-Bromo-2-oxo-pyrrolidin-1-yl)benzoic acid benzyl esterHCID 69484365—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07164016B2
出典データセットuspto-grants-2007_01
ORD IDord-72bb3e4e60cc414a964cc1fb33f65dc1
出典メモuspto-grants-2007_01