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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 599501Generated: October 29, 2026

Oxalyl chloride → HCID 90858244, compound

https://huagongshe.com/reaction/599501

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 67273507HCID 67273507—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 90858244HCID 90858244100.4%

Reaction Steps

To a stirred suspension of 2-cyano-3-(1-ethoxycarbonylmethyl-1H-indol-3-yl)-acrylic acid (3.0 g, 10 mmol) in dry dichloromethane (120 ml), in the presence of a few drops of dry DMF, was added oxalyl chloride (1.7 ml, 20 mmol). After stirring at rt overnight, the volatiles were removed under reduced pressure, the residue azeotoped twice with dry toluene and dried in vacuo, affording crude title compound (3.18 g) in quantitative yield. This material was stored under argon and was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897788B2
Source datasetuspto-grants-2011_03
ORD IDord-35931fe472674880b7f25d8408d8c542
Source noteuspto-grants-2011_03