HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiourea → 2-(Methylsulfonyl)phenylmethyl carbamimidothioate hydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | 1-(Bromomethyl)-2-methanesulfonylbenzene | HCID 18922474 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(Methylsulfonyl)phenylmethyl carbamimidothioate hydrobromide | HCID 13282655 | — |
Reaction Steps
A solution of 36.5 g of 2-(methylsulfonyl)benzyl bromide and 11.4 g of thiourea in 500 ml absolute ethanol was stirred at reflux temperature for 11/2 hours and then allowed to cool to room temperature. Upon standing, the solution yielded white feather-like crystals which were collected by filtration, washed with cold 1-chlorobutane, and dried in vacuo. The yield of 2-(methylsulfonyl)phenylmethyl carbamimidothioate hydrobromide, m.p. 203°-206° C., was 36.3 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04420325 |
| Source dataset | uspto-grants-1983_12 |
| ORD ID | ord-3bd0ba768f62497e82cdbb646d03e9fc |
| Source note | uspto-grants-1983_12 |