関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | Benzyl p-aminobenzoate | HCID 98488 | — |
| 反応物 | 2,4-Dibromobutyryl chloride | HCID 4413143 | — |
| 反応物 | 1-Butanaminium, N,N,N-tributyl-, carbonic acid (1:1) | HCID 11012140 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | (3-Bromo-2-oxo-pyrrolidin-1-yl)benzoic acid benzyl ester | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07164016B2 |
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| 出典データセット | uspto-grants-2007_01 |
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| ORD ID | ord-72bb3e4e60cc414a964cc1fb33f65dc1 |
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| 出典メモ | uspto-grants-2007_01 |
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