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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2418646Generated: November 1, 2026

Oxalyl chloride → HCID 20444701, compound

https://huagongshe.com/reaction/2418646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 13079828HCID 13079828—
SolventDichloromethaneHCID 6344—
ProductHCID 20444701HCID 2044470197.8%

Reaction Steps

Oxalyl chloride (11.52 gms) in dry methylene dichloride (10 ml) was slowly added to a suspension of 5-(p-chlorophenyl)-2-methyl-3-pyridine carboxylic acid (10 g) in dry methylene dichloride (50 ml). After standing for 1 hour at room temperature, the mixture was concentrated and the residue washed with dry diethyl ether, collected and dried to give 5-(p-chlorophenyl)-2-methyl-3-chlorocarbonylpyridine hydrochloride (11.95 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04473395
Source datasetuspto-grants-1984_09
ORD IDord-11ed6346027f4fa4b580ba0c507d2277
Source noteuspto-grants-1984_09