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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666694Generated: October 30, 2026

Hydrochloric Acid → 1-[4-(Trifluoromethoxy)phenyl]cyclopropane-1-carboxylic acid

https://huagongshe.com/reaction/1666694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant1-PyrrolidinamineHCID 27946—
ReactantHCID 57970159HCID 57970159—
SolventMethanolHCID 887—
Product1-[4-(Trifluoromethoxy)phenyl]cyclopropane-1-carboxylic acidHCID 45925732—

Reaction Conditions

Temperature78 °C

Reaction Steps

A mixture of 1-(4-trifluoromethoxyphenyl)cyclopropanecarbonitrile (4.0 g), 25% aqueous sodium hydroxide (0.46 mL), 30% aqueous hydrogen peroxide (25 mL), and methanol (100 mL) was heated at 55° C. for 1 h with stirring. The reaction mixture was concentrated under reduced pressure, the precipitated crystals were collected by filtration, to obtain white solid 1-(4-(trifluoromethoxy)phenyl)cyclopropanecarbamide (4.5 g). (3) A mixture of 1-(4-trifluoromethoxyphenyl)cyclopropanecarbamide (4.5 g), 15% aqueous sodium hydroxide (150 mL), and methanol (60 mL) was heated at 78° C. for 18 h with stirring. The reaction mixture was left stand for cooling, then the reaction solution was adjusted to pH 2 using 15% hydrochloric acid and concentrated under reduced pressure. The precipitated crystals were collected by filtration to obtain white solid 1-(4-(trifluoromethoxy)phenyl)cyclopropanecarboxylic acid (4.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044068B2
Source datasetuspto-grants-2011_10
ORD IDord-bd54535b29eb4a03a597ddecc8df4e78
Source noteuspto-grants-2011_10