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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1747034Generated: November 1, 2026

Thionyl Chloride → Methyl 5-(chloromethyl)thiophene-3-carboxylate

https://huagongshe.com/reaction/1747034

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantMethyl 5-(hydroxymethyl)thiophene-3-carboxylateHCID 12926498—
SolventDichloromethaneHCID 6344—
ProductMethyl 5-(chloromethyl)thiophene-3-carboxylateHCID 12926494—

Reaction Steps

To a mixed liquid of 4.86 g of methyl 5-(hydroxymethyl)thiophene-3-carboxylate and 50 ml of dichloromethane was added 4.12 ml of thionyl chloride under ice-cooling, followed by stirring at room temperature for 15 hours. The reaction solution was concentrated, added with ethyl acetate, and then washed with a saturated aqueous sodium hydrogen carbonate solution and a saturated aqueous sodium chloride solution. After drying over anhydrous magnesium sulfate, the solvent was then evaporated to obtain 4.90 g of methyl 5-(chloromethyl)thiophene-3-carboxylate as a pale yellow oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150541B2
Source datasetuspto-grants-2015_10
ORD IDord-d1766dbe06d046e5935b915ad1e9749f
Source noteuspto-grants-2015_10