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Sodium hydride → 2-cyano-3-hydroxy-N-(4-trifluoromethylphenyl)-hexa-2,5-dienamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | 2-Cyano-N-[4-(trifluoromethyl)phenyl]acetamide | HCID 3823803 | — |
| 反応物 | But-3-enoyl Chloride | HCID 10975427 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 2-cyano-3-hydroxy-N-(4-trifluoromethylphenyl)-hexa-2,5-dienamide | HCID 67789015 | 31.2% |
反応手順
6.0 g (0.026 mole) of 4'-trifluoromethyl-cyanoacetanilide in 200 ml of dry tetrahydrofuran were stirred under nitrogen at room temperature and were treated with 1.95 g (0.065 mole) of sodium hydride 80% oil dispersion. The mixture was stirred for a further 30 minutes at room temperature and cooled to -50° C. before the dropwise addition of 3.3 g (0.033 mole) of 3-butenoyl chloride prepared as described in J. Chem. Soc. (1948), p. 661. The mixture was stirred at -50° C. for 2 hours, then was poured onto dilute hydrochloric acid/ice and filtered. The solid was chromatographed over silica gel eluting with dichloromethane to give 2.4 g (31%) of the title compound as colorless crystals and 3 g of starting material were recovered.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05308865 |
| 出典データセット | uspto-grants-1994_05 |
| ORD ID | ord-ae91e35cfcff40ed9346a51457c95d8c |
| 出典メモ | uspto-grants-1994_05 |