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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1090810Generated: November 1, 2026

Ethyl vinyl ether → HCID 54481174, compound

https://huagongshe.com/reaction/1090810

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl vinyl etherHCID 8023—
ReactantEthoxalyl chlorideHCID 20884—
ProductHCID 54481174HCID 54481174—

Reaction Steps

145 g of ethyl vinyl ether were added dropwise to 137 g of ethyl chloroformylformate with cooling using ice/common salt; after warming to room temperature, the mixture was stirred for a further 20 hours. The volatile components were removed by distillation, and the residue was fractionated in a water-pump vacuum. Ethyl 4-ethoxy-2-oxobut-3-enoate of boiling point 140°-143° C./13 torr were obtained. 17.5 g of product were dissolved in 200 ml of toluene. 17.5 g of 2,6-dichlorophenylhydrazine were added at 0° C. with stirring. The mixture was slowly heated to boiling, and ethanol and water were removed in a water separator until the boiling point remained constant at 111° C. The residue was diluted with toluene, washed twice with 2N hydrochloric acid, saturated hydrogen carbonate solution and water, dried, evaporated to dryness and recrystallized from ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05082949
Source datasetuspto-grants-1992_01
ORD IDord-5872ae775d7649ee82102e25fd546855
Source noteuspto-grants-1992_01