Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913802Generated: November 1, 2026

Hydrochloric Acid → 4-[(4E)-3-(4-Carboxybenzyl)-5-(2-{4-[4-(trifluoromethyl)phenoxy]butoxy}phenyl)pent-4-en-1-yl]benzoic acid

https://huagongshe.com/reaction/1913802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-PropanolHCID 1031—
ReactantPotassium HydroxideHCID 14797—
ReactantMethyl 4-[(4E)-3-(4-cyanobenzyl)-5-(2-{4-[4-(trifluoromethyl)phenoxy]butoxy}phenyl)pent-4-en-1-yl]benzoateHCID 59180514—
SolventWaterHCID 962—
Product4-[(4E)-3-(4-Carboxybenzyl)-5-(2-{4-[4-(trifluoromethyl)phenoxy]butoxy}phenyl)pent-4-en-1-yl]benzoic acidHCID 59180485—

Reaction Conditions

Temperature110 °C

Reaction Steps

A solution of 450 mg (0.72 mmol) of methyl 4-[(4E)-3-(4-cyanobenzyl)-5-(2-{4-[4-(trifluoromethyl)phenoxy]butoxy}phenyl)pent-4-en-1-yl]benzoate in 15 ml of 1-propanol and 2 ml of water is mixed with 1207 mg (21.5 mmol) of potassium hydroxide and stirred at 110° C. for 12 h. After cooling, the mixture is acidified with 1 M hydrochloric acid, and the crystals which have separated out are filtered off with suction, washed several times with water and dried. 447 mg (0.65 mmol, 90% of theory, purity 92%) of the title compound are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609727B2
Source datasetuspto-grants-2013_12
ORD IDord-a5dfe1f4a375494ab7a3e9e088b94852
Source noteuspto-grants-2013_12