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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2115655Generated: November 1, 2026

Sodium Hydroxide → 3-(benzyloxy)-2-thiophenecarboxylic acid

https://huagongshe.com/reaction/2115655

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactantmethyl 3-(benzyloxy)-2-thiophenecarboxylateHCID 2764114—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product3-(benzyloxy)-2-thiophenecarboxylic acidHCID 276673391.3%

Reaction Steps

To a solution of methyl 3-(benzyloxy)-2-thiophenecarboxylate (7.85 g, 31.61 mmol) in MeOH (32 mL) and THF (16 mL) was added 2 N NaOH (21 mL), and the mixture was stirred at reflux for 10 hrs, and then concentrated under reduced pressure. The residue was diluted with water, washed with ether. The separated aqueous phase was acidified with 5N HCl. The precipitated solid was collected by filtration, washed with hexane, and dried under reduced pressure at 60° C. to give 3-(benzyloxy)-2-thiophenecarboxylic acid as a yellow solid (6.76 g, yield; 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435743B2
Source datasetuspto-grants-2008_10
ORD IDord-deab883940ce49a0bd6c946e4e540d37
Source noteuspto-grants-2008_10