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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1683838Generated: October 26, 2026

Tetrahydrofuran → 3-Chloro-4-methoxybenzoyl chloride

https://huagongshe.com/reaction/1683838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantOxalyl chlorideHCID 65578—
Reactant3-Chloro-p-anisic acidHCID 169982—
SolventChloroformHCID 6212—
Product3-Chloro-4-methoxybenzoyl chlorideHCID 4769299—

Reaction Steps

A stirred solution of 0.22 gram (0.0012 mole) of 3-chloro-4-methoxybenzoic acid in a small amount of tetrahydrofuran and chloroform was cooled to 0° C., and 0.12 mL (0.0014 mole) of oxalyl chloride was added dropwise. Upon completion of addition, the reaction mixture was allowed to warm to ambient temperature, where it was stirred for about 3.5 hours. After this time the reaction mixture was concentrated under reduced pressure, yielding 3-chloro-4-methoxybenzoyl chloride, which was dissolved in a small amount of tetrahydrofuran for later use.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05639763
Source datasetuspto-grants-1997_06
ORD IDord-0486d7e71bd341848c7455704c1e7c5c
Source noteuspto-grants-1997_06