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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1288076Generated: October 26, 2026

Methanol → 3(2,2-Dichlorovinyloxy)benzyl alcohol

https://huagongshe.com/reaction/1288076

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantSodium 4-methylbenzenesulfonateHCID 3720192—
Reactant1-(Bromomethyl)-3-[(2,2-dichloroethenyl)oxy]benzeneHCID 20482706—
SolventTolueneHCID 1140—
Product3(2,2-Dichlorovinyloxy)benzyl alcoholHCID 53679295—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture 3(2,2-dichlorovinyloxy)benzyl bromide (2.8 g), sodium p-toluene sulphonate (2.0 g) and methanol (20 ml) is warmed to 50° C for 1 hour, after which water (20 ml) and toluene (20 ml) is added with agitation. The toluene layer is separated, washed with water and concentrated by evaporation of the solvent under reduced pressure. The concentrate is then added dropwise to a 15% (w/v) aqueous solution of potassium hydroxide (100 ml) and the mixture warmed to 60° C for 1 hour, cooled to the ambient temperature and extracted with a mixture of toluene (10 ml) and methyl iso-butylketone (10 ml), the extracts dried over anhydrous magnesium sulphate and the solvents evaporated under reduced pressure to yield 3(2,2-dichlorovinyloxy)benzyl alcohol as a residual pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03987079
Source datasetuspto-grants-1976_10
ORD IDord-d4b0acb217a148afa27594fab3a846f4
Source noteuspto-grants-1976_10