HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 56613771, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Benzonitrile, 4-isothiocyanato- | HCID 17626 | — |
| Reactant | Methanesulfonamide | HCID 72879 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 56613771 | HCID 56613771 | — |
Reaction Steps
A mixture of 5 g (0.31 mol) of 4-cyanophenyl isothiocyanate, of 3.8 g (0.04 mol) of methylsulfonamide 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 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 to produce N-(4-cyanophenyl)-N'-methylsulfonyl-S-methylisothiourea.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04921939 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-e7a2f6040ea44c279d39e2dcfc5b3381 |
| Source note | uspto-grants-1990_05 |