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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1983064Generated: November 1, 2026

Thionyl Chloride → HCID 23149199, compound

https://huagongshe.com/reaction/1983064

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 23149157HCID 23149157—
SolventChloroformHCID 6212—
ProductHCID 23149199HCID 23149199—

Reaction Conditions

Temperature0 °C

Reaction Steps

The obtained 1-hydroxymethyl-4-trifluoromethyl-3-ethoxycarbonyl-1H-pyrole was dissolved to 3 ml of chloroform, and 4 ml of thionyl chloride was added, followed by refluxing for 30 minutes. After the reaction mixture was cooled to 0° C., it was poured into ice-water. The mixture was extracted with ethyl acetate. The organic layer was washed with saturated aqueous solution of sodium hydrogen carbonate, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under reduced pressure to obtain 225 mg of 1-chloromethyl-4-trifluoromethyl-3-ethoxycarbonyl-1H-pyrole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07541374B2
Source datasetuspto-grants-2009_06
ORD IDord-3e3c2a64ab56459f8bb3c94b096bc4ab
Source noteuspto-grants-2009_06