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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412227Generated: October 29, 2026

Benzyl Bromide → methyl 3-(benzyloxy)-2-thiophenecarboxylate

https://huagongshe.com/reaction/412227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Hydroxy-thiophene-2-carboxylic acid methyl esterHCID 581127—
SolventAcetoneHCID 180—
Productmethyl 3-(benzyloxy)-2-thiophenecarboxylateHCID 2764114100.8%

Reaction Steps

A mixture of methyl 3-hydroxy-2-thiophenecarboxylate (5.00 g, 31.61 mmol), benzyl bromide (3.76 mL, 31.61 mmol), and K2CO3 (4.81 g, 34.77 g) in acetone (50 mL) was stirred at reflux for 1.5 hrs. After cooled to room temperature, the mixture was filtered, and the filtrate was concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=15/1 to 9/1) to give methyl 3-(benzyloxy)-2-thiophenecarboxylate as a pale yellow oil (7.91 g, yield: quant.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562811B1
Source datasetuspto-grants-2003_05
ORD IDord-75cf4f4eec564476b9452795719d4ce0
Source noteuspto-grants-2003_05