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ChemicalBook--->CAS DataBase List--->144539-77-5

144539-77-5

144539-77-5 Structure

144539-77-5 Structure
IdentificationBack Directory
[Name]

((S)-piperidin-3-yl)methanol
[CAS]

144539-77-5
[Synonyms]

3(S)-Piperidinemethanol
(S)-Piperidine-3-methanol
(3S)-3-PiperidineMethanol
3-Piperidinemethanol, (3S)-
(3S)-piperidin-3-ylMethanol
((S)-piperidin-3-yl)methanol
(S)-3-Hydroxymethyl-piperidine, 99.8%ee, 98%
[Molecular Formula]

C6H13NO
[MDL Number]

MFCD10567175
[MOL File]

144539-77-5.mol
[Molecular Weight]

115.17
Chemical PropertiesBack Directory
[Boiling point ]

240.4±0.0 °C(Predicted)
[density ]

0.951
[refractive index ]

1.451
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[pka]

14.93±0.10(Predicted)
[Appearance]

Colorless to light yellow Solid-liquid mixture
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H332-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
Hazard InformationBack Directory
[Uses]

((S)-piperidin-3-yl)methanol is used to study enzymic chemoselective and enantioselective acyl transfers in hydroxymethylpiperidines.
[Synthesis]

Ethyl (3S)-piperidine-3-carboxylate

37675-18-6

3-Piperidinemethanol

4606-65-9

General procedure for the synthesis of 3-hydroxymethylpiperidine from ethyl (S)-3-piperidinecarboxylate: lithium aluminum hydride (LAH, 118 mL, 1.0 M in ether, 1.0 equiv.) was slowly added to a solution of tetrahydrofuran (THF, 250 mL) of the product of step A (18.5 g, 0.125 mmol) over a period of 20 min at 0 °C. The reaction mixture was gradually warmed to room temperature and subsequently heated to reflux for 2 hours. Upon completion of the reaction, it was cooled to room temperature and the reaction was quenched by slow addition of saturated sodium sulfate (Na2SO4) solution. The resulting slurry was dried by the addition of anhydrous sodium sulfate (Na2SO4), filtered through diatomaceous earth and concentrated to give a colorless oily product (13.7 g, 98% crude yield). The product was detected by chemical ionization mass spectrometry (CIMS) showing a molecular ion peak (MH+) of 116; the specific optical rotation ([α]20D) was -8.4° (determined by dissolving 5.0 mg of the sample in 2 mL of methanol).

[References]

[1] Patent: US2003/229099, 2003, A1. Location in patent: Page 174
[2] Patent: US2004/122018, 2004, A1. Location in patent: Page 208
[3] Patent: EP1140904, 2005, B1. Location in patent: Page/Page column 33
[4] Patent: EP1553074, 2005, A1. Location in patent: Page/Page column 37
[5] Patent: WO2014/173855, 2014, A1. Location in patent: Page/Page column 17
Spectrum DetailBack Directory
[Spectrum Detail]

((S)-piperidin-3-yl)methanol(144539-77-5)1HNMR
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