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(Triphenylphosphoranylidene)acetonitrile → (E)-Methyl 4,5-dichloro-2-(2-cyanovinyl)benzoate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | (Triphenylphosphoranylidene)acetonitrile | HCID 85524 | — |
| 反応物 | Methyl 4,5-dichloro-2-formylbenzoate | HCID 86647797 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | (E)-Methyl 4,5-dichloro-2-(2-cyanovinyl)benzoate | HCID 86647796 | — |
反応手順
A mixture of the product from Example 56C (2.0 g, 8.6 mmol) and (triphenylphosphoranylidene)acetonitrile (2.87 g, 9.5 mmol) in toluene (30 mL) was refluxed for 24 hours. The reaction was cooled to room temperature and filtered through a short plug of silica gel eluting with diethyl ether to remove the triphenyl phosphine oxide. The filtrate was concentrated and the residue was purified via flash chromatography on a silica gel column (5:95 ethyl acetate:hexane) to afford the title compound and the corresponding Z isomer. 1H NMR (300 MHz, DMSO-d6) δ ppm 3.88 (s, 3H) 6.55 (d, J=16.27 Hz, 1H) 8.05 (d, J=16.95 Hz, 1H) 8.09 (s, 1H) 8.13 (s, 1H); MS (DCI+) m/z 273.0 [M+H]+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08846951B2 |
| 出典データセット | uspto-grants-2014_09 |
| ORD ID | ord-6fbeb336356947ea9aa4ad3a0f377ec9 |
| 出典メモ | uspto-grants-2014_09 |