HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Chloride → Benzyl ethanimidothioate--hydrogen chloride (1/1)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Thioacetamide | HCID 2723949 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Benzyl ethanimidothioate--hydrogen chloride (1/1) | HCID 12626231 | 85% |
Reaction Steps
A mixture of thioacetamide (15.0 g, 0.20 mol) and benzyl chloride (25.3 g, 0.20 mol) in chloroform (75 ml) was heated under reflux for 90 minutes (the thioacetamide required ˜40 minutes to go into solution). The reaction mixture was then allowed to cool to room temperature and was then stood at 0° C. overnight, when colourless crystals formed as a layer on the surface. The product was filtered off, washed with cold 10% ether-chloroform and sucked dry to give the title compound (25.55 g) as colourless prisms. Mpt.=161°-163° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USRE039576E1 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-84278d0b88bd47148b38faca86770b5f |
| Source note | uspto-grants-2007_04 |