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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596575Generated: October 30, 2026

Ethanol → p-Ethoxycarbonylbenzoyl chloride

https://huagongshe.com/reaction/596575

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantTerephthaloyl chlorideHCID 7488—
SolventBenzeneHCID 241—
Productp-Ethoxycarbonylbenzoyl chlorideHCID 12276626—

Reaction Steps

p-Ethoxycarbonylbenzoyl chloride is prepared according to the method of M. J. Dewar and J. P. Schroeder, J. Org. Chem., 30, 2297 (1965), by the gradual addition of a small amount of ethyl alcohol to a boiling solution of terephthaloyl chloride in benzene. After removal of the solvent the residue is distilled under reduced pressure to give the acyl chloride which boils at 102°-105° C. at 0.4 mm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04011236
Source datasetuspto-grants-1977_03
ORD IDord-a7b530671e9640e78a772d5fe112c8ba
Source noteuspto-grants-1977_03