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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1199198Generated: November 3, 2026

Oxalyl chloride → HCID 14539525, compound

https://huagongshe.com/reaction/1199198

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 numberUS04898949
Source datasetuspto-grants-1990_02
ORD IDord-412c35837fa34f6793271b539aa011b5
Source noteuspto-grants-1990_02