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Water → N-((Phenylmethoxy)carbonyl)-L-serine methyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Dimethyl Sulfate | HCID 6497 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | N-(Benzyloxycarbonyl)-L-serine | HCID 100310 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | N-((Phenylmethoxy)carbonyl)-L-serine methyl ester | HCID 6999535 | — |
反応手順
N-CBZ-L-serine (25 g) was dissolved in 100 ml of dry N,N-dimethylformamide at 0° C. under argon. Triethylamine (2 e.g., 30 ml) and dimethylsulfate (20 ml) were added. The contents of the vessel were stirred overnight at room temperature and then poured into 500 ml of water and extracted with ethyl acetate (3×200 ml). The organic layer was washed with water and brine and dried with sodium sulfate. Rotary evaporation afforded an oil which crystallized after silica gel chromatography in pure ethyl ether. The structure of the product, N-CBZ-L-serine methyl ester, was confirmed by NMR spectroscopy.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04676989 |
| 出典データセット | uspto-grants-1987_06 |
| ORD ID | ord-49d76b88f95e44b78687b03e026d330d |
| 出典メモ | uspto-grants-1987_06 |