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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611131Generated: November 3, 2026

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

https://huagongshe.com/reaction/1611131

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 numberUS06984649B1
Source datasetuspto-grants-2006_01
ORD IDord-0ecba36891bc40ec9f723c7cbb154691
Source noteuspto-grants-2006_01