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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412228Generated: October 29, 2026

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

https://huagongshe.com/reaction/412228

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 numberUS06562811B1
Source datasetuspto-grants-2003_05
ORD IDord-d8052d36ca3b42e9b280de495f70cb7d
Source noteuspto-grants-2003_05