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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 130272Generated: October 31, 2026

4-Hydroxybenzoic Acid → 4-({6-[(3-Ethyloxetan-3-YL)methoxy]hexyl}oxy)benzoic acid

https://huagongshe.com/reaction/130272

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydroxybenzoic AcidHCID 135—
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant3-{[(6-Bromohexyl)oxy]methyl}-3-ethyloxetaneHCID 59207310—
SolventWaterHCID 962—
Product4-({6-[(3-Ethyloxetan-3-YL)methoxy]hexyl}oxy)benzoic acidHCID 5976759666.4%

Reaction Steps

A dimethylformamide (3 L) solution of 3-[(6-bromohexyloxy)methyl]-3-ethyloxetane 500 g, 4-hydroxybenzoic acid 297 g and potassium carbonate 490 g was stirred at 90° C. for 8 hours. Water 4 L was added to the reaction mixture, and then it was extracted with toluene 4 L. The organic layer was washed with water, and the solvent was distilled off. Sodium hydroxide 200 g, water 1 L and ethanol 2.5 L were added to the resulting residue and refluxed for 4 hours. Ethanol (1 L) was distilled off at atmospheric pressure, and then the solution was acidified by hydrochloric acid to obtain a slurry. The slurry was filtered and dried to thereby obtain 400 g of 4-[6-(3-ethyloxetane-3-ylmethoxy)hexyloxy]benzoic acid. Melting point: 58.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07381350B2
Source datasetuspto-grants-2008_06
ORD IDord-2a05641a385e4dafafa03acb0082da18
Source noteuspto-grants-2008_06