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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 492197Generated: October 29, 2026

Oxalyl chloride → HCID 86596413, compound

https://huagongshe.com/reaction/492197

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 68969741HCID 68969741—
SolventDichloromethaneHCID 6344—
ProductHCID 86596413HCID 86596413115%

Reaction Conditions

Temperature22 °C

Reaction Steps

0.6 cm3 (6.88 mmol) of oxalyl chloride is added to a suspension, cooled to a temperature in the region of 5° C., of 0.74 g (2.28 mmol) of 3-carboxy-1-(quinol-8-yl)-1H-indole hydrochloride in 15 cm3 of dichloromethane under an argon atmosphere. After stirring at a temperature in the region of 22° C. for 15 hours, the reaction mixture is concentrated to dryness under reduced pressure (2.7 kPa) to give 0.9 g of 3-chlorocarbonyl-1-(quinol-8-yl)-1H-indole hydrochloride in the form of a yellow solid which is used directly in the following step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531663B2
Source datasetuspto-grants-2009_05
ORD IDord-61c35ab6062b42559d986cfb96c34b20
Source noteuspto-grants-2009_05