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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323690Generated: October 27, 2026

Hydrochloric Acid → 3-(4-(Trifluoromethyl)benzamido)propyloxyphenol

https://huagongshe.com/reaction/323690

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
Reactant3-(4-(Trifluoromethyl)benzamido)propyloxyphenyl benzoateHCID 86754495—
SolventWaterHCID 962—
Product3-(4-(Trifluoromethyl)benzamido)propyloxyphenolHCID 8675449494%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of 0.87 g of 3-ethyl-5-methyl-4-(3-(4-(trifluoromethyl)benzamido)propyloxyphenyl benzoate and 10 ml of methanol was added a mixture of 0.16 g of sodium hydroxide and 2 m of water, while stirring at 0° C. After stirring at room temperature for 24 hours, the reaction mixture was made weak acidic by the addition of 10% hydrochloric acid, and extracted with 50 ml of ethyl acetate. The ethyl acetate layer was washed with saturated saline solution, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure to give a residue. The residue was subjected to silica gel chromatography, which afforded 0.66 g of 3-ethyl-5-methyl-4-(3-(4-(trifluoromethyl)benzamido)propyloxyphenol (94% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06214835B1
Source datasetuspto-grants-2001_04
ORD IDord-cdf1e3aa33c043e3ade040d9bac596ec
Source noteuspto-grants-2001_04