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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1268837Generated: November 1, 2026

Oxalyl chloride → HCID 73446015, compound

https://huagongshe.com/reaction/1268837

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant3-Cyano-3-(2-thienyl)acrylic acid potassium saltHCID 53396629—
SolventDichloromethaneHCID 6344—
ProductHCID 73446015HCID 7344601594.8%

Reaction Steps

To a stirring solution of oxalyl chloride (81.17 mL, 0.93 mol) in CH2Cl2 (350 mL) was added 3-cyano-3-thiophen-2-yl-acrylic acid potassium salt 21 (100 g, 0.45 mol) portion-wise over 20 min. An additional 250 mL of CH2Cl2 were added to assist stirring. The slurry was stirred at room temperature for 30 min and was then filtered. The potassium chloride salts were washed with copious CH2Cl2. Collected organic rinses were combined and solvent removed under vacuum to afford 84.3 g of 22, which was carried on to the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199119B2
Source datasetuspto-grants-2007_04
ORD IDord-6a1e7f69cb0948ac861297e01f5782f8
Source noteuspto-grants-2007_04