Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 468579Generated: October 30, 2026

1-Aminocyclopropane-1-carboxylic acid → 1-({[4-Cyano-3-(trifluoromethyl)phenyl]carbamoyl}amino)cyclopropanecarboxylic acid

https://huagongshe.com/reaction/468579

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Aminocyclopropane-1-carboxylic acidHCID 535—
ReactantSodium HydroxideHCID 14798—
Reactant4-Isocyanato-2-(trifluoromethyl)benzonitrileHCID 11063739—
SolventAcetoneHCID 180—
SolventDiethyl EtherHCID 3283—
Product1-({[4-Cyano-3-(trifluoromethyl)phenyl]carbamoyl}amino)cyclopropanecarboxylic acidHCID 6675181650%

Reaction Steps

A solution of 4-isocyanato-2-(trifluoromethyl)benzonitrile (4.56 g, 21.5 mmol) in acetone (12 ml) is added dropwise to 1-aminocyclopropane carboxylic acid (2.02 g, 20 mmol) dissolved in an aqueous solution of sodium hydroxide (12 ml, 0.8 g, 20 mmol). The reaction medium is stirred for 1 hour at ambient temperature then poured into an aqueous solution of sodium hydroxide (1N, 40 ml). The solution obtained is washed with ethyl acetate (30 ml) then acidified by the addition of an aqueous solution of sulphuric acid (2M, 30 ml) and extracted with ethyl acetate (2×50 ml). The organic phase thus obtained is washed with water then with a saturated aqueous solution of sodium chloride, dried over Na2SO4 and filtered. The solvent is evaporated off under reduced pressure. The residue obtained is taken up in ethyl ether in order to produce a white solid, after filtration, with a yield of 50% (3.16 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08624037B2
Source datasetuspto-grants-2014_01
ORD IDord-395366e3bd8740c1b1a977b472dbab2e
Source noteuspto-grants-2014_01