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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1288074Generated: October 30, 2026

3-(2,2,2-Trichloro-1-acetoxy-ethoxy)-toluene → 1-[(2,2-Dichloroethenyl)oxy]-3-methylbenzene

https://huagongshe.com/reaction/1288074

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(2,2,2-Trichloro-1-acetoxy-ethoxy)-tolueneHCID 20568927—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
Product1-[(2,2-Dichloroethenyl)oxy]-3-methylbenzeneHCID 20568926—

Reaction Steps

By a metallic reductive dehydrohydrogenation method. 1(3-tolyloxy)-2,2,2-trichloroethyl acetate (14.2 g) was dissolved in glacial acetic acid (40 ml) and zinc dust (3.6 g) was slowly added to the solution was stirring at the ambient temperature. The temperature rose to 60° C in response to the exothermic reaction which occurred, after which the mixture was heated at 50°-60° C for 4 hours. The mixture was filtered and the filtrate poured in an excess of water and extracted with chloroform. The extracts were washed twice with water, with saturated sodium bicarbonate solution, and finally with water. After drying the chloroform extracts over anhydrous magnesium-sulphate, the solvent was removed by evaporation under reduced pressure and the residual oil distilled to yield crude 3-tolyl 2,2-dichlorovinyl ether, collected as a fraction boiling at 92°-95° C/0.3 mm, which was redistilled and the fraction boiling at 84° C/0.2 mm Hg collected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03987079
Source datasetuspto-grants-1976_10
ORD IDord-fdb2e081480c48e08350c51ff4449bd0
Source noteuspto-grants-1976_10