Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368632Generated: October 30, 2026

Hydrochloric Acid → HCID 66862425, compound

https://huagongshe.com/reaction/2368632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant18-Crown-6HCID 28557—
Reactant1-(4-(Trifluoromethyl)phenyl)ethan-1-oneHCID 69731—
ReactantPropanoic acid, 2-methoxy-, methyl esterHCID 86599—
ReactantPotassium tertbutoxideHCID 50987170—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66862425HCID 66862425—

Reaction Steps

10.14 g Potassium-tert.-butoxide and 225 mg 1,4,7,10,13,16-hexaoxacyclooctadecan are dissolved in 80 ml tetrahydrofurane. Then a solution of 10.0 g 1-(4-Trifluoromethyl-phenyl)-ethanone in 40 ml of tetrahydrofurane and a solution of 12.6 g racemic 2-Methoxy-propionic acid methyl ester in 40 ml of tetrahydrofurane are simultaneously added dropwise. After completion of addition the mixture is heated for four hours to reflux, cooled to 0° C. and hydrolyzed by dropwise addition of 50 ml of a 4 M solution of hydrochloric acid. The residue is partitioned between water and ethylacetate and the phases are separated. The aqueous phase is twice extracted with ethylacetate and the combined organic phases are washed with brine. After drying with magnesium sulphate the solvents are evaporated in vacuo. The residue is chromatographed on silica gel (cyclohexane/ethylacetate 95:5 to 85:15).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703793B2
Source datasetuspto-grants-2014_04
ORD IDord-d1dac388a28141df8c04d3328711df17
Source noteuspto-grants-2014_04