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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757959Generated: October 26, 2026

Ethanol → HCID 12854007, compound

https://huagongshe.com/reaction/1757959

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSulfuric AcidHCID 1118—
Reactant2,3-Dichloro-4-(4-hydroxybenzoyl)phenoxyacetic acidHCID 12854004—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 12854007HCID 1285400793%

Reaction Steps

An 85.38 g. (0.25 mole) portion of 2,3-dichloro-4-(4'-hydroxybenzoyl)phenoxyacetic acid, 34.5 g. (0.75 mole) of ethanol, and 100 ml. of ethylene dichloride, using 3.5 ml. of sulfuric acid as the catalyst was mixed and refluxed with stirring overnight according to the procedure of Clinton and Laskowski, J.A.C.S. 70 3135, 1948. The acid gradually went into solution. The reaction layer was cooled, separated and the organic layer washed successively with water, twice with KHCO3 solution and finally with water. The dried ethylene dichloride was evaporated to dryness to give an oil which solidified to give 86 g. crude ester on trituration with pentane and filtering; m.p. 127°-9° (93% yield). This material was used without further purification in subsequent experiments.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04371546
Source datasetuspto-grants-1983_02
ORD IDord-a4862225352a4b7d8ca04d4b57639282
Source noteuspto-grants-1983_02