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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165303Generated: November 2, 2026

Oxalyl chloride → HCID 14539525, compound

https://huagongshe.com/reaction/2165303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 14539524HCID 14539524—
SolventDichloromethaneHCID 6344—
ProductHCID 14539525HCID 14539525—

Reaction Steps

To a solution of dry (0.1 mmHg at 80° C.) 3,3.bis(4-fluorophenyl)-2-(1-methyl-1H-tetrazol-5-yl)-2-propenoic acid 3.8 g (11.0 mmoles) in 20 mL of dry methylene chloride was added 4 mL (46.0 mmoles) of purified oxalyl chloride (redistilled over CaH2) in one single portion. The reaction mixture was warmed gradually to reflux temperature for two hours. The mixture was evaporated under reduced pressure to remove volatile solvent then excess oxalyl chloride was removed under vacuum (20 mmHg) at ambient temperature for 2 hours and under high vacuum (0.1 mmHg) at 50° C. for 16 hours to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04939265
Source datasetuspto-grants-1990_07
ORD IDord-37885326d0e44cd3a1455a679ae30386
Source noteuspto-grants-1990_07