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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1388847Generated: November 2, 2026

3-(Trifluoromethyl)phenol → m-Trifluoromethylphenyl 1-amidino-4-piperidinepropionate hydrochloride

https://huagongshe.com/reaction/1388847

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)phenolHCID 7376—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-Amidino-4-piperidinepropionic acid hydrochlorideHCID 15583512—
SolventPyridineHCID 1049—
Productm-Trifluoromethylphenyl 1-amidino-4-piperidinepropionate hydrochlorideHCID 7050831362.1%

Reaction Steps

A mixture of 4.0 g of 1-amidino-4-piperidinepropionic acid hydrochloride and 2.75 g of m-trifluoromethylphenol was suspended in 27 ml of dry pyridine. To the suspension was added 3.5 g of dicyclohexylcarbodiimide, and the resulting mixture was stirred at room temperature for 6 hours. After removal of any insoluble materials, the solvent was removed. The residue was washed with ether, dissolved in chloroform and then stirred. After removal of any insoluble materials, the filtrate was washed twice with a saturated sodium chloride solution and then dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure to obtain 4.0 g (yield: 62.0%) of m-trifluoromethylphenyl 1-amidino-4-piperidinepropionate hydrochloride as colorless crystals having a melting point of 97° to 100° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04433152
Source datasetuspto-grants-1984_02
ORD IDord-cd0940ffb03942e794163208124b35a5
Source noteuspto-grants-1984_02