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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110316Generated: November 1, 2026

1-Bromooctadecane → HCID 19389007, compound

https://huagongshe.com/reaction/1110316

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromooctadecaneHCID 8218—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 53653037HCID 53653037—
ReactantHCID 54411747HCID 54411747—
SolventMethanolHCID 887—
ProductHCID 19389007HCID 1938900795%

Reaction Steps

A mixture of 2.54 g (12.8 mmol) of 3-hydroxy-5-methylthiobenzoic acid methyl ester, 4.7 g (14.1 mmol) of 1-bromooctadecane and 2.7 g (19.2 mmol) of potassium carbonate in 60 ml of anhydrous DMP was stirred and heated at 80° under an argon atmosphere for 21 hours. The reaction mixture was filtered through a Celite pad and the filtrate was concentrated at reduced pressure. Water was added to the residue and the product was filtered and recrystallized from methylene chloride-methanol to give 5.5 g (95% yield), mp 64°-66°, of 3-(methylthio)-5-(octadecyloxy)benzoic acid methyl ester. The nmr and mass spectra were consistent with the structure. A solution of 2.7 g (6 mmol) of 3-(methylthio)-5-(octadecyloxy)benzoic acid methyl ester and 5.0 ml (30 mmol) of 6 N NaOH in 125 ml of methanol was stirred at reflux under argon for 5 hours. The solvent was removed at reduced pressure, the residue was acidified with 6 N HCl and the product was extracted with chloroform. The dried extract was concentrated to a solid which was triturated with hexane and filtered to give 2.6 g, mp 90°-92°, of 3-(methylthio)-5-(oxtadecyloxy)benzoic acid. The nmr and mass spectra were consistent with the structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05324747
Source datasetuspto-grants-1994_06
ORD IDord-c45171a33cc646749f8ecc3e568431da
Source noteuspto-grants-1994_06