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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380593Generated: October 30, 2026

Benzyl Bromide → 3,4-Bis(benzyloxy)benzoic acid

https://huagongshe.com/reaction/1380593

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantPotassium HydroxideHCID 14797—
ReactantEthyl 3,4-DihydroxybenzoateHCID 77547—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventMethyl Ethyl KetoneHCID 6569—
Product3,4-Bis(benzyloxy)benzoic acidHCID 10854155183.1%

Reaction Steps

To 60 g (0.33 mole) of ethyl 3,4-dihydroxybenzoate in 50 ml of methyl ethyl ketone was added 105.5 g (0.76 mole) of K2CO3 and 168.8 g (0.76 mole) of benzyl bromide. The mixture was refluxed for 16 hours and filtered. Evaporation of the filtration gave an oil. This oil was mixed with 40 g of KOH, 350 ml of water and 350 ml of methanol and refluxed for 2.5 hours. The methanol was evaporated and the reaction mixture was acidified with concentrated HCl. The precipitate was filtered to give 101 g (92%) of the desired product; m.p. 184°-185° C. The NMR and IR spectra were consistent with the assigned structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04582855
Source datasetuspto-grants-1986_04
ORD IDord-021a0977eb8b49808214f3fb1bbbba45
Source noteuspto-grants-1986_04