HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-Dichloropropene → (4-Bromophenyl)(2-chloroallyl)sulfane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-Dichloropropene | HCID 6565 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Bromothiophenol | HCID 66049 | — |
| Product | (4-Bromophenyl)(2-chloroallyl)sulfane | HCID 14819351 | 67% |
Reaction Steps
According to the procedure of W. K. Anderson et al., J. Chem. Soc., Perkin 1, 1 (1976) a mixture of 4-bromothiophenol (40.0 g, 0.211 mol) and K2CO3 (35.3 g, 0.254 mol) was heated at reflux for 1 hour. 2,3-Dichloro-1-propene (23.5 g, 0.211 mol) was added. The resulting mixture was heated at reflux for 2 hours, cooled and concentrated. The mixture was diluted with H2O and extracted with ether (3×150 mL). The combined extracts were dried (MgSO4), and concentrated to give an oil. Distillation under high vacuum gave 37.2 g (67%) of product as a colorless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04895860 |
| Source dataset | uspto-grants-1990_01 |
| ORD ID | ord-aabe4721e9b941f08963a1cf7f68b8b1 |
| Source note | uspto-grants-1990_01 |