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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2305065Generated: October 31, 2026

Hydrochloric Acid → 3,5-Diethyl-4-(4-(2,2-diethoxyethoxy)butyloxy)phenol

https://huagongshe.com/reaction/2305065

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
Reactant3,5-Diethyl-1-benzoyloxy-4-(4-(2,2-diethoxyethoxy)butyloxy)benzeneHCID 18429649—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product3,5-Diethyl-4-(4-(2,2-diethoxyethoxy)butyloxy)phenolHCID 1842953294%

Reaction Steps

To a solution of 31.0 g of 3,5-diethyl-1-benzoyloxy-4-(4-(2,2-diethoxyethoxy)butyloxy)benzene dissolved in 100 ml of methanol was added a solution of 5.1 g of potassium hydroxide dissolved in 25 g of water. After stirring at room temperature for 1 hour, the reaction mixture was acidified by the addition of diluted hydrochloric acid, and concentrated. The residue was poured into water, and extracted twice with ethyl acetate. The ethyl acetate layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0.60 g (yield, 94%) of 3,5-diethyl-4-(4-(2,2-diethoxyethoxy)butyloxy)phenol, nD25.0 1.4890.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06437184B1
Source datasetuspto-grants-2002_08
ORD IDord-da694d7a23c14604a437420810a7eae0
Source noteuspto-grants-2002_08