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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334423Generated: October 30, 2026

Trifluoroacetic acid → HCID 68276432, compound

https://huagongshe.com/reaction/334423

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTetramethylammonium Triacetoxyborohydride (>90%)HCID 13696215—
Reactant4,4-DifluorocyclohexanoneHCID 15789092—
Reactant2-Amino-4-(4-methylpiperazin-1-yl) benzoic acid tertbutyl esterHCID 66735920—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 68276432HCID 68276432102.9%

Reaction Steps

1.045 ml (13.57 mmol) of trifluoroacetic acid, 1 g (7.46 mmol) of 4,4-difluorocyclohexanone and 2.158 g (8.20 mmol) of tetramethylammonium triacetoxyborohydride are added to 1.521 g (5.22 mmol) of tert-butyl 2-amino-4-(4-methylpiperazin-1-yl)benzoate dissolved in 60 ml of dichloromethane. The reaction is left under stirring at room temperature for 24 hours. The solvent is evaporated and then the crude reaction product is redissolved in 30 ml of ethyl acetate. The solution is successively washed with 0.5 M HCl solution, 0.5 M soda solution and finally with saturated NaHCO3 solution. The organic phase is dried on sodium sulfate, filtered and concentrated to obtain 2.2 g of tert-butyl 2-(4,4-difluorocyclohexylamino)-4-(4-methylpiperazin-1-yl)benzoate in the form of a light brown gum (yield=72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883821B2
Source datasetuspto-grants-2014_11
ORD IDord-5e4afa93d1ae490380ce34cb5b9fb56b
Source noteuspto-grants-2014_11