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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767315Generated: November 3, 2026

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

https://huagongshe.com/reaction/1767315

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 numberUS07232909B2
Source datasetuspto-grants-2007_06
ORD IDord-0ebbba650ecd4a05973aa171e7b3b36f
Source noteuspto-grants-2007_06