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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757844Generated: October 25, 2026

Benzyl Bromide → Methyl 3,5-bis(benzyloxy)benzoate

https://huagongshe.com/reaction/1757844

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 3,5-DihydroxybenzoateHCID 75076—
SolventDimethylformamideHCID 6228—
ProductMethyl 3,5-bis(benzyloxy)benzoateHCID 2733652160.4%

Reaction Steps

A mixture of 25.0 g (0.15 mol) of 3,5-dihydroxybenzoic acid methyl ester, 44 ml (0.37 mol) of benzyl bromide and 82 g (0.60 mol) of potassium carbonate in 300 ml of DMF was stirred and heated at 85° under argon for 45 hours. The cooled reaction mixture was filtered and the filtrate was concentrated at reduced pressure. The residue was treated with methylene chloride and the extract was filtered again to remove salts. Crystallization from methylene chloride-methanol gave 41.9 g (81% yield, mp 64°-66°) of 3,5-bis(phenylmethoxy)benzoic acid methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05446189
Source datasetuspto-grants-1995_08
ORD IDord-85912af37a5e46089cb2f44eece6ed93
Source noteuspto-grants-1995_08