HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiourea → HCID 20456549, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | 1-(1-Bromoethyl)-2-nitrobenzene | HCID 12643460 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20456549 | HCID 20456549 | 85.2% |
Reaction Steps
A solution of 33.5 g of 1-(2-nitrophenyl)ethyl bromide and 11.4 g of thiourea in 375 ml absolute ethanol was stirred at reflux temperature for 31/2 hours. The reaction mixture was allowed to cool to room temperature and was concentrated to one-half volume in vacuo. The solution was then cooled to ca. -60° C. and 1-chlorobutane was added until a gummy solid formed. The supernatant was decanted and the residue dried in vacuo to give 38 g of 1-(2-nitrophenyl)ethyl carbamimidothioate hydrobromide as a light orange solid which was not further purified.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04420325 |
| Source dataset | uspto-grants-1983_12 |
| ORD ID | ord-9f56934293f34c828195a38ba7428bed |
| Source note | uspto-grants-1983_12 |