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Trifluoroacetic acid → 4-Methyl-4-(p-nitrobenzyloxycarbonyl)aminovaleric acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Trifluoroacetic acid | HCID 6422 | — |
| 反応物 | Anisole | HCID 7519 | — |
| 反応物 | 4-Methyl-4-p-nitrobenzyloxycarbonylaminovaleric acid p-methoxybenzyl ester | HCID 53971933 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | 4-Methyl-4-(p-nitrobenzyloxycarbonyl)aminovaleric acid | HCID 13334384 | — |
反応手順
A mixture of 4-methyl-4-p-nitrobenzyloxycarbonylaminovaleric acid p-methoxybenzyl ester (25 g), anisole (25 g) and trifluoroacetic acid (125 ml) was stirred for 15 minutes at room temperature. Evaporation of trifluoroacetic acid gave an oily residue which was then dissolved in diethyl ether. The ether solution was extracted with aqueous sodium carbonate. The aqueous layer was washed with diether ether, acidified with dilute hydrochloric acid and extracted with benzene. The benzene extract was washed with water, dried over anhydrous sodium sulfate and evaporated to give 4-methyl-4-p-nitrobenzyloxycarbonylaminovaleric acid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04742052 |
| 出典データセット | uspto-grants-1988_05 |
| ORD ID | ord-ee09b96d6f97420b9c4ef0a3e6050de5 |
| 出典メモ | uspto-grants-1988_05 |