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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611130Generated: November 3, 2026

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

https://huagongshe.com/reaction/1611130

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 numberUS06984649B1
Source datasetuspto-grants-2006_01
ORD IDord-3e3816af37224e3d855890a70f0b2f71
Source noteuspto-grants-2006_01