HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Pyridinemethanol → O-[(Pyridin-3-yl)methyl] (4-cyanophenyl)carbamothioate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Pyridinemethanol | HCID 7510 | — |
| Reactant | Benzonitrile, 4-isothiocyanato- | HCID 17626 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | O-[(Pyridin-3-yl)methyl] (4-cyanophenyl)carbamothioate | HCID 12790266 | 43.5% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04156780 |
| Source dataset | uspto-grants-1979_05 |
| ORD ID | ord-a466d27218384f8aa65905f1c4d56569 |
| Source note | uspto-grants-1979_05 |