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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058548Generated: October 27, 2026

Potassium Hydroxide → 2-Thiophenecarboxylic acid, 4-bromo-3-methoxy-

https://huagongshe.com/reaction/1058548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantMethyl 4-bromo-3-methoxythiophene-2-carboxylateHCID 2736824—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product2-Thiophenecarboxylic acid, 4-bromo-3-methoxy-HCID 54226795.6%

Reaction Steps

A solution of 37.5 g (0.15 mole) of methyl 4-bromo-3-methoxy-2-thiophenecarboxylate and 12 g of KOH (0.18 mole) in a mixture of 250 mL of methanol and 100 mL of water was refluxed for 2 hr. The reaction mixture was cooled and most of the methanol was removed in vacuo. The solution was partitioned with ether and dilute aqueous HCl. The organic phase was separated dried over MgSO4, filtered and concentrated and dried under a vacuum to give 34 g (94%) of a colorless solid. mp 191-192° C. 1H NMR (300 MHz, CDCl3): δ 7.5 (s, 1H); 4.1 (s, 3H). Anal. Calc'd for C6H5BrO3S: C, 30.04; H, 2.23; S, 13.52. Found: C, 29.89; H, 2.06; S, 13.14.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06518222B2
Source datasetuspto-grants-2003_02
ORD IDord-503f48f7f89f429582518edbcc2e6109
Source noteuspto-grants-2003_02