化工社化工社 化学情報印刷レポート · 研究参考用
Tetrahydrofuran → tert-Butyl (S)-(4-hydroxy-1-methoxybutan-2-yl)carbamate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | Lithium borohydride | HCID 4148881 | — |
| 反応物 | (S)-3-tert-Butoxycarbonylamino-4-methoxy-butyric acid benzyl ester | HCID 57976545 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | tert-Butyl (S)-(4-hydroxy-1-methoxybutan-2-yl)carbamate | HCID 53259998 | — |
反応手順
A solution of (S)-3-tert-Butoxycarbonylamino-4-methoxy-butyric acid benzyl ester (10.4 g, 32.3 mmol) in dry diethylether (70 ml) cooled to 0° C. is treated slowly with a 2.0 M solution of LiBH4 in THF (32.2 ml, 64.4 mmol). The reaction mixture is allowed to warm to ambient temperature and then left to stir. After 6 hours the reaction mixture is quenched slowly with 0.5 M aqueous solution of citric acid and extracted with ether. The ether phase is dried over magnesium sulphate and evaporated. The crude product is purified by flash silica chromatography (elution with a gradient 3:7 to 6:4 ethylacetate/hexane) to afford ((S)-3-Hydroxy-1-methoxymethyl-propyl)-carbamic acid tert-butyl ester as a clear oil. [M-BOC] 120.13
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07288537B2 |
| 出典データセット | uspto-grants-2007_10 |
| ORD ID | ord-21cdab5396d74da699493784cc7af339 |
| 出典メモ | uspto-grants-2007_10 |