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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593915Generated: November 1, 2026

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

https://huagongshe.com/reaction/1593915

Reaction equation

Participants

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

Reaction Conditions

Temperature90 °C

Reaction Steps

First stage: A solution prepared by dissolving 500 g of 3-[(6-bromohexyloxy)methyl]-3-ethyloxetane, 297 g of 4-hydoxybenzoic acid and 490 g of potassium carbonate in 3 L of dimethylforamide was stirred at 90° C. for 8 hours. After adding 4 L of water to the reaction mixture, it was extracted with 4 L of toluene. The organic layer was washed with water, and then the solvent was distilled off. Added to the resulting residue were 200 g of sodium hydroxide, 1 L of water and 2.5 L of ethanol, and the mixture was refluxed for 4 hours. Ethanol 1 L was distilled off at an 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 numberUS07300604B2
Source datasetuspto-grants-2007_11
ORD IDord-5958c7f071e84ed7af3ac059efc2ff9c
Source noteuspto-grants-2007_11