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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1792799Generated: November 3, 2026

Oxalyl chloride → HCID 22024947, compound

https://huagongshe.com/reaction/1792799

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 22024962HCID 22024962—
SolventDichloromethaneHCID 6344—
ProductHCID 22024947HCID 2202494786.9%

Reaction Conditions

Temperature22 °C

Reaction Steps

0.45 mL (5.16 mmol) of oxalyl chloride is added to a solution, cooled to a temperature in the region of 5° C., of 0.45 g (1.64 mmol) of 3-carboxy-1-(quinol-8-yl)-1H-pyrrole hydrochloride in 20 mL 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), then it is placed under an argon atmosphere and 20 mL of dichloromethane and 0.45 mL (5.16 mmol) of oxalyl chloride are successively added. After stirring at a temperature in the region of 22° C. for 15 hours, concentrating the reaction medium to dryness under reduced pressure (2.7 kPa) gives 0.418 g of 3-chlorocarbonyl-1-(quinol-8-yl)-1H-pyrrole hydrochloride in the form of a cream-coloured solid which is used directly in the following step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07078414B2
Source datasetuspto-grants-2006_07
ORD IDord-53e910dc6ecf4007b8f1e9f0503f1f12
Source noteuspto-grants-2006_07