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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1492836Generated: October 30, 2026

1-Bromooctadecane → 3-Hydroxy-5-(octadecyloxy)benzoic acid phenylmethyl ester

https://huagongshe.com/reaction/1492836

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromooctadecaneHCID 8218—
ReactantPotassium CarbonateHCID 11430—
Reactant3,5-Dihydroxybenzoic acid phenylmethyl esterHCID 11299537—
SolventAcetoneHCID 180—
SolventDimethylformamideHCID 6228—
Product3-Hydroxy-5-(octadecyloxy)benzoic acid phenylmethyl esterHCID 1523347636%

Reaction Steps

A mixture of 30 g (0.123 mol) of 3,5-dihydroxybenzoic acid phenylmethyl ester, 40.9 g (0.123 mol) of 1-bromooctadecane, 17 g (0.123 mol) of anhydrous potassium carbonate in 500 ml of acetone and 10 ml of DMF was stirred at reflux for 25 hours. The reaction mixture was filtered and the filtrate was concentrated at reduced pressure to a solid. The residue was treated with water and the product was extracted with methylene chloride. The dried extract was concentrated at reduced pressure to a solid which was purified by HPLC using 1% ethyl acetate-methylene chloride to give 22 g (36% yield, mp 72°-75°) of 3-hydroxy-5-(octadecyloxy)benzoic acid phenylmethyl ester. The structure was confirmed by nmr and mass spectra.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05374772
Source datasetuspto-grants-1994_12
ORD IDord-128d7b99917041a4a2b0cca0e2463789
Source noteuspto-grants-1994_12