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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177865Generated: November 1, 2026

Benzyl Bromide → Benzyl 3-(furan-3-yl)-2-methoxy-6-(phenylthiomethyl)benzoate

https://huagongshe.com/reaction/2177865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(Furan-3-yl)-2-methoxy-6-(phenylthiomethyl)benzoic acidHCID 67108027—
SolventTetrahydrofuranHCID 8028—
ProductBenzyl 3-(furan-3-yl)-2-methoxy-6-(phenylthiomethyl)benzoateHCID 6710772291.5%

Reaction Steps

A solution of 3-(furan-3-yl)-2-methoxy-6-(phenylthiomethyl)benzoic acid (Intermediate 223, 0.83 g), benzyl bromide (0.46 g) and potassium carbonate (0.55 g) in THF (15 ml) was heated to 60° C. for 8 hours. After cooling, the mixture was filtered and the filtrate was evaporated to dryness. The residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane with a gradient of 0-10% to give benzyl 3-(furan-3-yl)-2-methoxy-6-(phenylthiomethyl)-benzoate (0.96 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067905B2
Source datasetuspto-grants-2015_06
ORD IDord-aa75b827b2c94b7e87494ad912cdb2dd
Source noteuspto-grants-2015_06