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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154801Generated: October 30, 2026

Ethylene Glycol → Ethyl 2-hydroxyimino-3,3-ethylenedioxy-4-chlorobutyrate

https://huagongshe.com/reaction/1154801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantHCID 178472915HCID 178472915—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventBenzeneHCID 241—
ProductEthyl 2-hydroxyimino-3,3-ethylenedioxy-4-chlorobutyrateHCID 8673808758.9%

Reaction Steps

A mixture of ethyl 2-hydroxyimino-3-oxo-4-chlorobutyrate (syn isomer, 10 g), ethylene glycol (16 g), p-toluenesulfonic acid (0.3 g) and dried benzene (100 ml) was heated for 19 hours under reflux while removing water azeotropically. After the reaction mixture was cooled to ambient temperature, water (30 ml) and benzene (20 ml) were added thereto. The mixture was saturated with sodium chloride and the benzene layer was separated, and the remaining aqueous layer was further extracted with benzene (20 ml). The benzene layer and extract were combined together, washed with a saturated aqueous solution of sodium chloride (30 ml×2), dried over magnesium sulfate and then filtered. The filtrate was evaporated to give an oil of ethyl 2-hydroxyimino-3,3-ethylenedioxy-4-chlorobutyrate (syn isomer, 7.23 g). (Yield: 58.9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04298529
Source datasetuspto-grants-1981_11
ORD IDord-012073b718eb41d89b8be2b8156d4c62
Source noteuspto-grants-1981_11