ChemicalBook--->CAS DataBase List--->1245724-46-2

1245724-46-2

1245724-46-2 Structure

1245724-46-2 Structure
IdentificationBack Directory
[Name]

(S)-Tetrahydro-2H-pyran-3-amine hydrochloride
[CAS]

1245724-46-2
[Synonyms]

(S)-TETRAHYDRO-2H-PYRAN-3-AMINE HCL
(S)-Tetrahydro-2H-pyran-3-amine hydrochloride
(S)-Tetrahydro-2H-pyran-3-amine 2hydrochloride
2H-Pyran-3-amine, tetrahydro-, hydrochloride (1:1), (3S)-
(S)-tetrahydro-2H-pyran-3-amine hydrochloride(WXC09058S1)
[Molecular Formula]

C5H12ClNO
[MDL Number]

MFCD09056862
[MOL File]

1245724-46-2.mol
[Molecular Weight]

137.61
Chemical PropertiesBack Directory
[storage temp. ]

Store at room temperature, keep dry and cool
[Appearance]

Off-white to light brown Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)Corrosion (GHS05)
GHS07,GHS05
[Signal word ]

Danger
[Hazard statements ]

H302-H335-H318-H315
[Precautionary statements ]

P280-P305+P351+P338-P310-P264-P280-P302+P352-P321-P332+P313-P362-P264-P270-P301+P312-P330-P501
Spectrum DetailBack Directory
[Spectrum Detail]

(S)-Tetrahydro-2H-pyran-3-amine hydrochloride(1245724-46-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

Carbamic acid, N-[(3S)-tetrahydro-2H-pyran-3-yl]-, 1,1-dimethylethyl ester

1295722-66-5

(S)-Tetrahydro-2H-pyran-3-amine hydrochloride

1245724-46-2

General procedure for the synthesis of (S)-3-aminotetrahydropyran hydrochloride from the compound (CAS: 1295722-66-5): the intermediate (S)-tert-butyltetrahydro-2H-pyran-3-ylcarbamate (414 g, 2.06 mol) was added to a methanolic solution (4 L) of 6 N HCl, and the reaction mixture was stirred at room temperature until the reaction was complete (monitored by TLC monitoring). Upon completion of the reaction, the mixture was concentrated under vacuum to afford 283 g of (S)-(tetrahydropyran-3-yl)amine hydrochloride as a white solid (99.8% yield, enantiomeric excess >99%). The structure of the product was confirmed by 1H NMR (400 MHz, DMSO-d6): δ 8.37 (s, 3H), 3.87-3.72 (m, 1H), 3.70-3.57 (m, 1H), 3.54-3.38 (m, 2H), 3.12 (d, J = 2.1 Hz, 1H), 2.05-1.89 (m, 1H), 1.81 -1.60 (m, 2H), 1.49 (dtd, J = 12.5, 8.3, 4.3 Hz, 1H).

[References]

[1] Patent: WO2013/7768, 2013, A1. Location in patent: Page/Page column 110; 111
[2] Synlett, 2013, vol. 24, # 8, p. 987 - 990
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