関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 1-Phenethylamine, (+)- | HCID 643189 | — |
| 反応物 | 2-(2-Oxopyrrolidin-1-yl)butanoic acid | HCID 10464751 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | (R)-1-Phenylethanamine (S)-2-(2-oxopyrrolidin-1-yl)butanoate | HCID 44140303 | 97.8% |
反応手順
A solution of (R)-alpha-methylbenzylamine (106 g) and triethylamine (89 g) in toluene (100 ml) was added to a suspension of (RS)-alpha-ethyl-2-oxo-1-pyrrolidineacetic acid (300 g, 1.75 mol) in toluene (1 L). The mixture was heated until complete dissolution, cooled to room temperature and stirred for 3 hours. The solids were filtered and rinsed with toluene (300 ml) to give 250 g of (s)-alpha-ethyl-2-oxo-1-pyrrolidineacetic acid (R)-alpha-methylbenzylamine salt. The solids were crystallized from toluene and 205 g (yield 41%) of (S)-alpha-ethyl-2-oxo-1-pyrrolidineacetic acid (R)-alpha-methylbenzylamine salt was obtained. The isolated solid was treated with hydrochloric acid solution and the enantiomerically pure (S)-alpha-ethyl-2-oxo-1-pyrrolidineacetic acid could be isolated in 90% yield.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07902380B2 |
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| 出典データセット | uspto-grants-2011_03 |
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| ORD ID | ord-f6523e3307784bdab6a95afdba9aa4d4 |
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| 出典メモ | uspto-grants-2011_03 |
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