Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1576232Generated: October 31, 2026

Acetic Acid → 3-(2,2-Dichlorovinyloxy)-benzaldehyde

https://huagongshe.com/reaction/1576232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrochloric AcidHCID 313—
ReactantHexamethylenetetramineHCID 4101—
Reactant1-(Bromomethyl)-3-[(2,2-dichloroethenyl)oxy]benzeneHCID 20482706—
SolventWaterHCID 962—
SolventCarbon TetrachlorideHCID 5943—
Product3-(2,2-Dichlorovinyloxy)-benzaldehydeHCID 13489976—

Reaction Steps

3(2,2-Dichlorovinyloxy)benzyl bromide (2.5 g) was carefully added to a stirred solution of hexamethylene tetramine (2.1 g) in carbon tetrachloride (20 ml) at the ambient temperature. After five minutes the precipitate was collected by filtration and washed with acetone. The solid thus obtained was added to aqueous acetic acid solution (50% by weight, 16 ml) and the mixture refluxed for one hour. A mixture of water (16 ml) and concentrated hydrochloric acid (4.5 ml) was then added and the mixture refluxed for a further 15 minutes. After cooling the mixture was extracted with chloroform, the extracts washed with water (twice), dried over anhydrous magnesium sulphate and the solvent removed by evaporation under reduced pressure to yield a residue of substantially pure 3(2,2-dichlorovinyloxy)benzaldehyde, identification of which was confirmed by infra-red and nuclear magnetic resonance spectroscopy.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03979519
Source datasetuspto-grants-1976_09
ORD IDord-3539d6de2a4241268b49c19bd4ad316e
Source noteuspto-grants-1976_09