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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330281Generated: October 29, 2026

2,3-Dichloropropene → (4-Bromophenyl)(2-chloroallyl)sulfane

https://huagongshe.com/reaction/330281

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-DichloropropeneHCID 6565—
ReactantPotassium CarbonateHCID 11430—
Reactant4-BromothiophenolHCID 66049—
Product(4-Bromophenyl)(2-chloroallyl)sulfaneHCID 1481935167%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04895860
Source datasetuspto-grants-1990_01
ORD IDord-aabe4721e9b941f08963a1cf7f68b8b1
Source noteuspto-grants-1990_01