Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463905Generated: October 30, 2026

Hydrochloric Acid → Phenol, 4-(2,2-dichloroethenyl)-

https://huagongshe.com/reaction/463905

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantTetraethylammoniumHCID 5413—
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantTriethylazanium chlorideHCID 12698378—
SolventWaterHCID 962—
ProductPhenol, 4-(2,2-dichloroethenyl)-HCID 532490195.2%

Reaction Steps

A 10 ml quantity of concentrated hydrochloric acid, 2.5 g of tetraethyl ammonium salt of p-toluenesulfonic acid and 5.5 g of triethyl ammonium chloride were dissolved in 60 ml of ethanol. The solution was placed in an anode chamber and a cathode chamber separated from each other by a diaphragm. In the cathode chamber was further introduced 10 m mole of p-hydroxyphenyl trichloromethyl carbinol ##STR6## Then constant-current electrolysis was performed with use of lead as a cathode and carbon as an anode. After current (5 F/mole) was passed, the reaction liquid from the cathode chamber was added to 200 ml of water. The mixture was extracted four times with 50 ml of hexane. Then the extract was dried over anhydrous magnesium sulfate. The solvent was distilled off and the residue was purified by silica gel column chromatography, giving 1.80 g of p-hydroxy-β,β-dichlorostyrene ##STR7## Yield 95.2%, m.p. 90°-91° C. IR (cm-1) 3370, 1604, 1500, 1442, 1375, 1235, 1180, 1109, 909, 873, 821, 682.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04544766
Source datasetuspto-grants-1985_10
ORD IDord-940e57a83357473c904f523c36bf5794
Source noteuspto-grants-1985_10