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3-Pyridinemethanol → O-[(Pyridin-3-yl)methyl] (4-cyanophenyl)carbamothioate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3-Pyridinemethanol | HCID 7510 | — |
| 反応物 | Benzonitrile, 4-isothiocyanato- | HCID 17626 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | Thiourea | HCID 2723790 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | 1,2-Dimethoxyethane | HCID 8071 | — |
| 生成物 | O-[(Pyridin-3-yl)methyl] (4-cyanophenyl)carbamothioate | HCID 12790266 | 43.5% |
反応手順
To a solution of 3-pyridylcarbinol (2.18g., 0.02 mole) in 50 ml. of glyme there is added sodium hydride (0.87g. of a 57% oil dispersion, 0.02 mole). The solution is allowed to stand 2 hrs. and then p-cyanophenyl isothiocyanate (3.2g., 0.02 mole) in 50 ml. of glyme is added dropwise. The reaction mixture is stirred at room temperature for 18 hrs. It is then saturated with sodium bicarbonate and poured into an excess of water. The resulting suspension is filtered to give a solid residue which is recrystallized from toluene to give 2.3g. of solid melting at 153°-154° C., with decomposition. The thiourea structure is confirmed by infra-red spectroscopy. The product is obtained in a 43.5% yield.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04156780 |
| 出典データセット | uspto-grants-1979_05 |
| ORD ID | ord-a466d27218384f8aa65905f1c4d56569 |
| 出典メモ | uspto-grants-1979_05 |