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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488256Generated: October 27, 2026

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

https://huagongshe.com/reaction/488256

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromooctadecaneHCID 8218—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 11299537HCID 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 numberUS05298652
Source datasetuspto-grants-1994_03
ORD IDord-ab294117e5ce4f7cbb10f82e43eb63d4
Source noteuspto-grants-1994_03