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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009477Generated: October 30, 2026

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

https://huagongshe.com/reaction/1009477

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

4.86 g of methyl 5-(hydroxymethyl)thiophene-3-carboxylate was dissolved in 50.0 mL of dichloromethane, and 4.12 mL of thionyl chloride was added thereto under ice-cooling, followed by stirring at room temperature for 15 hours. The reaction liquid was concentrated under reduced pressure, and to the obtained residue was added ethyl acetate, and then washed with an aqueous saturated sodium hydrogen carbonate solution and saturated brine. It was dried over anhydrous magnesium sulfate, and then the solvent was evaporated to obtain 4.90 g of methyl 5-(chloromethyl)thiophene-3-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973078B2
Source datasetuspto-grants-2011_07
ORD IDord-54a1ca223ad44f0b89855ad551186b9b
Source noteuspto-grants-2011_07