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Benzyl chloroformate → N-((Phenylmethoxy)carbonyl)-L-serine methyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Benzyl chloroformate | HCID 10387 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | L-Serine, methyl ester, hydrochloride (1:1) | HCID 2723730 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | N-((Phenylmethoxy)carbonyl)-L-serine methyl ester | HCID 6999535 | 95% |
反応手順
To a solution of 24.01 g L-serine-methylester hydrochloride in 130 ml of water were added at 0° C. 29.8 g of benzyl chloroformate. The pH was kept at 6-7 by adding a 40% aqueous solution of sodium hydroxide. After 3 h at 0° C. the mixture was extracted with 5 portions of ethyl acetate, the combined extracts were dried and evaporated to give 37.12 g (95%) of pure methyl 3-hydroxy-(S)-2-benzyloxycarbonylamino-propionate. IR (neat): 3380 m (NH, OH), 1720 s, br. (C=O), 1540 s (amide II).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06130348 |
| 出典データセット | uspto-grants-2000_10 |
| ORD ID | ord-ff11aa4641b54591917c8f0b3a2e812a |
| 出典メモ | uspto-grants-2000_10 |