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1221793-42-5

1221793-42-5 Structure

1221793-42-5 Structure
IdentificationBack Directory
[Name]

(S)-1-(tert-butoxycarbonyl)-4,4-difluoropiperidine-2-carboxylic acid
[CAS]

1221793-42-5
[Synonyms]

(S)-1-(tert-butoxycarbonyl)-4,4-difluoropiperidine-2-carboxylic acid
(S)-l-(TERTBUTOXYCARBONYL)-4, 4-DIFLUOROPIPERIDINE-2-rARRHYVI TC ACTD
(2S)-1-[(tert-butoxy)carbonyl]-4,4-difluoropiperidine-2-carboxylic acid
(2S)-4,4-difluoro-1-[(2-methylpropan-2-yl)oxycarbonyl]piperidine-2-carboxylic acid
1,2-Piperidinedicarboxylic acid, 4,4-difluoro-, 1-(1,1-dimethylethyl) ester, (2S)-
[Molecular Formula]

C11H17F2NO4
[MDL Number]

MFCD03094869
[MOL File]

1221793-42-5.mol
[Molecular Weight]

265.25
Chemical PropertiesBack Directory
[Boiling point ]

356.4±42.0 °C(Predicted)
[density ]

1.27±0.1 g/cm3(Predicted)
[pka]

3.20±0.40(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501
Spectrum DetailBack Directory
[Spectrum Detail]

(S)-1-(tert-butoxycarbonyl)-4,4-difluoropiperidine-2-carboxylic acid(1221793-42-5)1HNMR
Hazard InformationBack Directory
[Synthesis]

1-(tert-butyl) 2-methyl (S)-4,4-difluoropiperidine-1,2-dicarboxylate

1352342-07-4

(S)-1-(tert-butoxycarbonyl)-4,4-difluoropiperidine-2-carboxylic acid

1221793-42-5

General procedure for the synthesis of (S)-1-(tert-butoxycarbonyl)-4,4-difluoropiperidine-2-carboxylic acid from compound (CAS: 1352342-07-4): compound 2 (1.526 g, 5.462 mmol) was dissolved in tetrahydrofuran (11 mL), methanol (11 mL), and 1N aqueous potassium hydroxide (11 mL, 11 mmol). It was stirred at room temperature for 1.5 hours. Subsequently, 1N aqueous potassium hydroxide solution (5.5 mL, 5.5 mmol) was added and stirring was continued for 1 hour. After completion of the reaction, the mixture was concentrated to half the original volume, diluted with water and washed once with ether. The aqueous phase was acidified with 1N hydrochloric acid (20 mL) and extracted twice with ethyl acetate. The organic phases were combined, washed once with saturated brine, dried over anhydrous sodium sulfate and concentrated to give compound 3 (1.429 g, 98% yield). Mass spectrometry analysis showed [M-H]? = 264.2.

[References]

[1] Patent: WO2011/156610, 2011, A2. Location in patent: Page/Page column 102
[2] Patent: CN106928127, 2017, A. Location in patent: Paragraph 0232; 0243; 0244; 0245; 0246; 0247
[3] Patent: WO2015/5901, 2015, A1. Location in patent: Page/Page column 528; 529
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