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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110280Generated: November 1, 2026

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

https://huagongshe.com/reaction/1110280

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromooctadecaneHCID 8218—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 3,5-DihydroxybenzoateHCID 75076—
SolventAcetoneHCID 180—
SolventDimethylformamideHCID 6228—
Product3-Hydroxy-5-(octadecyloxy)benzoic acid methyl esterHCID 1523347832.2%

Reaction Steps

A mixture of 50.0 g (0.297 mol) of methyl 3,5-dihydroxybenzoate, 99.2 g (0.297 mol) of 1-bromooctadecane and 41 g (0.297 mol) of potassium carbonate in 100 ml of acetone and 50 ml of DMF was stirred at reflux under argon for 24 hours. The solvents were removed at reduced pressure and the residue was heated with methylene chloride and filtered hot. The filtrate was concentrated at reduced pressure to a solid which was recrystallized from methylene chloride-methanol to give the 3,5-dialkylated product. The filtrate was concentrated to dryness and the residue was recrystallized from methylene chloride-methanol to give more of the dialkylated product. The filtrate was concentrated to dryness and recrystallized from ether-hexane to give 40.2 g (32% yield, mp 95°-97°) of 3-hydroxy-5-(octadecyloxy)benzoic acid methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05324747
Source datasetuspto-grants-1994_06
ORD IDord-b030237d87a74d9d983abd11c76f7601
Source noteuspto-grants-1994_06