HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 56637441, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Benzenesulfonamide | HCID 7370 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Benzonitrile, 4-isothiocyanato- | HCID 17626 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 56637441 | HCID 56637441 | 82.7% |
Reaction Steps
A mixture of 5 g (0.031 mol) of 4-cyanophenyl isothiocyanate, of 6.3 g (0.04 mol) of benzenesulfonamide in 50 cm3 of acetone and of 1.6 g (0.04 mol) of sodium hydroxide in 3 cm3 of water is maintained for two hours at room temperature. The precipitate obtained is filtered, washed with acetone and ethyl ether (2×20 cm3). The final solid (9 g; yield 94%) is then placed in 50 cm3 of 95% ethanol containing 2.75 cm3 (0.044 mol) of methyl iodide. After 24 hours at room temperature the solution is concentrated to dryness and the residue is washed with ethyl ether (3×20 cm3) and dried in vacuo. 8.5 g (yield 80%) of N-(4-cyanophenyl)-N'-phenylsulfonyl-S-methylisothiourea (melting point 150° C.) is obtained: ##STR23##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04877895 |
| Source dataset | uspto-grants-1989_10 |
| ORD ID | ord-67ffcb328f6248c295c4867e760d20f4 |
| Source note | uspto-grants-1989_10 |