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Dimethylformamide → 2-(4-Chlorophenyl)-3-methylbutanamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Benzeneacetic acid, 4-chloro-alpha-(1-methylethyl)- | HCID 16197 | — |
| 反応物 | Oxalyl chloride | HCID 65578 | — |
| 触媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | 2-(4-Chlorophenyl)-3-methylbutanamide | HCID 12898176 | — |
反応手順
To a solution of 4.25 g (20 mmol) of 2-(4-chlorophenyl)-3-methylbutanoic acid in 30 ml of ether containing one drop of N,N-dimethylformamide is added dropwise 3.81 g (30 mmol) of oxalyl chloride. The solution is stirred at RT until gas evolution ceases. The solvent and excess oxalyl chloride are removed in vacuo and the residue is taken up in 30 ml of ether. This solution is then added dropwise at 0°-5° to 4.86 g (40 mmol) of a 14% w/w aqueous solution of ammonia. After stirring the mixture for 30 minutes at 0°-5°, the aqueous layer is removed. The ethereal solution is washed with water, dried over sodium sulfate, filtered and concentrated in vacuo to obtain 2-(4-chlorophenyl)-3-methylbutyramide.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04254264 |
| 出典データセット | uspto-grants-1981_03 |
| ORD ID | ord-699f9ade6fb3410d9d6c32bd49ffb9fe |
| 出典メモ | uspto-grants-1981_03 |