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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1457528Generated: October 30, 2026

Methyl chloroformate → Methyl 5-methylthiophene-3-carboxylate

https://huagongshe.com/reaction/1457528

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
Reactant4-Bromo-2-methylthiopheneHCID 638584—
ProductMethyl 5-methylthiophene-3-carboxylateHCID 4644182—

Reaction Steps

Alternatively, initial lithiation of 3-bromo-5-methylthiophene followed by capture with methyl chloroformate gives methyl 5-methylthiophene-3-carboxylate. Free-radical bromination of the methyl group followed by treatment with an alkali azide, subsequent reduction and hydrolysis provides 5-(aminomethyl)thiophene-3-carboxylic acid (VI). ##STR38##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05849693
Source datasetuspto-grants-1998_12
ORD IDord-dd43a9d7e64b4608953bce55cb6f7edc
Source noteuspto-grants-1998_12