ChemicalBook--->CAS DataBase List--->886779-69-7

886779-69-7

886779-69-7 Structure

886779-69-7 Structure
IdentificationBack Directory
[Name]

3-Trifluoromethyl-piperazine-1-carboxylic acid tert-butyl ester
[CAS]

886779-69-7
[Synonyms]

1-Boc-3-(trifluoromethyl)piperazine
tert-butyl 3-(trifluoromethyl)piperazine-1-carboxylate
1-Piperazinecarboxylic acid, 3-(trifluoromethyl)-, 1,1-dimethylethyl ester
[Molecular Formula]

C10H17F3N2O2
[MOL File]

886779-69-7.mol
[Molecular Weight]

254.25
Chemical PropertiesBack Directory
[Boiling point ]

263.4±35.0 °C(Predicted)
[density ]

1.189±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[pka]

5.95±0.40(Predicted)
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

3-Trifluoromethyl-piperazine-1-carboxylic acid tert-butyl ester(886779-69-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

Di-tert-butyl dicarbonate

24424-99-5

2-(Trifluoromethyl)piperazine

131922-05-9

3-Trifluoromethyl-piperazine-1-carboxylic acid tert-butyl ester

886779-69-7

To a solution of 2-(trifluoromethyl)piperazine (135 mg, 0.876 mmol) in dichloromethane (6 mL) was added di-tert-butyl dicarbonate (0.224 mL, 0.963 mmol) and the reaction mixture was stirred for 3 hours at room temperature. After completion of the reaction, the mixture was concentrated and the residue was purified by silica gel column chromatography (eluent: 0-100% hexane solution of ethyl acetate) to afford 1-Boc-3-trifluoromethylpiperazine (200 mg, 0.787 mmol, 90% yield) as a light yellow solid. Mass spectrometry (ES+) analysis: the theoretical value of C10H17F3N2O2 was 254 and the measured value was 155 [M+H]+ - Boc group.

[References]

[1] Patent: WO2018/136887, 2018, A1. Location in patent: Page/Page column 122
[2] Patent: WO2014/175621, 2014, A1. Location in patent: Paragraph 662; 663; 664
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