HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → N-(4-cyanophenyl)-S-methylisothiourea hydroiodide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | (4-Cyanophenyl)thiourea | HCID 2757973 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | N-(4-cyanophenyl)-S-methylisothiourea hydroiodide | HCID 178504005 | 77.9% |
Reaction Steps
To a solution of 6.7 g (0.037 mol) of 4-cyanophenylthiourea in 150 cm3 of 2-butanone, 13.1 g (0.092 mol) of methyl iodide are added. After 24 hours of contact at room temperature, the solid formed is filtered, washed with 2-butanone (2×20 cm3) then with ethyl ether (2×50 cm3), which makes it possible to obtain 9.2 g (yield 76%; melting point 212° C.) of N-(4-cyanophenyl)-S-methylisothiourea hydroiodide: ##STR16##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04877895 |
| Source dataset | uspto-grants-1989_10 |
| ORD ID | ord-70ecfb888f68439bbbc88b994f9ee17e |
| Source note | uspto-grants-1989_10 |