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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1288075Generated: October 31, 2026

Sulfuric Acid → 1-[(2,2-Dichloroethenyl)oxy]-3-methylbenzene

https://huagongshe.com/reaction/1288075

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium HydroxideHCID 14798—
Reactant3-(2,2,2-Trichloro-1-acetoxy-ethoxy)-tolueneHCID 20568927—
SolventMethanolHCID 887—
Product1-[(2,2-Dichloroethenyl)oxy]-3-methylbenzeneHCID 20568926—

Reaction Conditions

Temperature15 °C

Reaction Steps

By an electrochemical reductive dehydrohalogenation method 1(3-tolyloxy)-2,2,2-trichloroethyl acetate (15.8 g), concentrated sulphuric acid (98% w/v, 9.8 g) and methanol (220 ml) was charged into an electrolytic cell, which was surrounded by a cooling bath set to maintain the temperature at about 15° C, and fitted with a cylindrical diaphragm, stirrer, reference electrode (SCE) and a working electrode. The cathode was a lead plate (surface area about 40 cm2). Using a current density in the range 5 to 10 mA/cm2 the reaction was conducted in the potential range -1100 to 1700 mV (SCE). When reduction was completed the cathodic electrolyte was neutralised with caustic soda and extracted with methylene chloride, the extracts dried over anhydrous sodium sulphate and evaporated to yield a residue of crude 3-tolyl 2,2-dichlorovinyl ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03987079
Source datasetuspto-grants-1976_10
ORD IDord-e45b5c5740264e4ab57e337f026041e3
Source noteuspto-grants-1976_10