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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2115654Generated: October 30, 2026

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

https://huagongshe.com/reaction/2115654

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 numberUS07435743B2
Source datasetuspto-grants-2008_10
ORD IDord-97983cb17a5140dfa95cf7701bbe04c7
Source noteuspto-grants-2008_10