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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248347Generated: October 27, 2026

Water → 4-[(4,5-Difluoro-2-methoxyphenoxy)methyl]-N-(triphenylmethyl)-1-piperidineethanamine

https://huagongshe.com/reaction/248347

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant(2-Bromoethyl)tritylamineHCID 15718287—
Reactant4-[(4,5-Difluoro-2-methoxyphenoxy)methyl]piperidine hydrochlorideHCID 19763367—
SolventDimethylformamideHCID 6228—
Product4-[(4,5-Difluoro-2-methoxyphenoxy)methyl]-N-(triphenylmethyl)-1-piperidineethanamineHCID 1976338541.5%

Reaction Conditions

Temperature90 °C

Reaction Steps

5.88 g (0.020 mol) of 4-[(4,5-difluoro-2-methoxyphenoxy)methyl]piperidine hydrochloride, 7.7 g (0.021 mol) of 2-bromo-N-(triphenylmethyl)ethylamine and 6.91 g (0.050 mol) of K2CO3 in 40 ml of DMF are reacted. The reaction mixture is heated to 90° C. for 8 hours. It is cooled to room temperature, poured into 500 ml of water and extracted 3 times with ethyl acetate. The organic phases are combined, washed with water, dried over MgSO4 and filtered, and the solvent is evaporated off under reduced pressure. The product is obtained in the form of an oil after chromatography. Yield: 41.5%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05210086
Source datasetuspto-grants-1993_05
ORD IDord-d32e64f01da745f7a4d7dbc8a579c938
Source noteuspto-grants-1993_05