Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 976283Generated: October 30, 2026

Water → 4'-(Benzyloxy)[1,1'-biphenyl]-4-carboxylic acid

https://huagongshe.com/reaction/976283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
Reactant4'-Hydroxy-4-biphenylcarboxylic acidHCID 301556—
SolventDimethylformamideHCID 6228—
Product4'-(Benzyloxy)[1,1'-biphenyl]-4-carboxylic acidHCID 14744793100%

Reaction Conditions

Temperature10 °C

Reaction Steps

4'-hydroxy 4-biphenylcarboxylic acid (5.0 g) was added to a stirred suspension of sodium hydride (60% w/w dispersion in mineral oil, 2.34 g) in dry dimethylformamide (45 ml) whilst maintaining the temperature of the reaction mixture below 10° C. The reaction mixture was stirred at 10° C. for 20 minutes. A solution of benzyl bromide (8.4 g) in dry dimethylformamide (10 ml) was added over a period of 10 minutes. The reaction mixture was stirred at 70° C. for 2 hours and the mixture was then poured into cold water (900 ml) to precipitate a solid. The solid was collected by filtration, washed with water (3×200 ml) and added to a mixture of 2M aqueous sodium hydroxide solution (100 ml) and ethanol (100 ml). The mixture was stirred at 100° C. for 12 hours. The ethanol was removed by evaporation and the aqueous residue taken to pH 1.0 by the addition of 12M aqueous hydrochloric acid solution to precipitate a solid. The solid was collected by filtration, washed with water (3×100 ml), ethyl acetate (3×100 ml) and dried to give 4'-benzyloxy-4-biphenylcarboxylic acid (100% yield) as a colourless solid, m.p. >300° C.; m/z 304 (M).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05612352
Source datasetuspto-grants-1997_03
ORD IDord-5bd4e2c9fac745a28303f62e73a52191
Source noteuspto-grants-1997_03