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167216-17-3

167216-17-3 Structure

167216-17-3 Structure
IdentificationBack Directory
[Name]

Carbamic acid, [(1R)-3-hydroxy-1-methylpropyl]-, 1,1-dimethylethyl ester (9CI)
[CAS]

167216-17-3
[Synonyms]

Boc-(R)-3-aminobutan-1-ol
N-Boc-(R)-3-aminobutan-1-ol
(R)-N-BOC-3-AMINOBUTAN-1-OL
N-(t-Butoxycarbonyl)-L-β-homoalaninol
tert-Butyl (R)-(4-hydroxybutan-2-yl)carbamate
(R)-tert-Butyl (4-hydroxybutan-2-yl)carbamate
(-)-tert-butyl [(R)-3-hydroxy-1-methylpropyl]carbamate
Carbamic acid, N-[(1R)-3-hydroxy-1-methylpropyl]-, 1,1-dimethylethyl ester
Carbamic acid, [(1R)-3-hydroxy-1-methylpropyl]-, 1,1-dimethylethyl ester (9CI)
[Molecular Formula]

C9H19NO3
[MDL Number]

MFCD18831346
[MOL File]

167216-17-3.mol
[Molecular Weight]

189.25
Chemical PropertiesBack Directory
[Boiling point ]

301.4±25.0 °C(Predicted)
[density ]

1.010±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,2-8°C
[pka]

12.32±0.46(Predicted)
[Appearance]

White to off-white Solid
[Optical Rotation]

Consistent with structure
[InChI]

InChI=1S/C9H19NO3/c1-7(5-6-11)10-8(12)13-9(2,3)4/h7,11H,5-6H2,1-4H3,(H,10,12)/t7-/m1/s1
[InChIKey]

JSZOAOLSEKSNTD-SSDOTTSWSA-N
[SMILES]

C(OC(C)(C)C)(=O)N[C@H](C)CCO
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

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

Carbamic acid, [(1R)-3-hydroxy-1-methylpropyl]-, 1,1-dimethylethyl ester (9CI)(167216-17-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

Methyl(R)-N-Boc-3-aminobutyrate

159877-47-1

Carbamic acid, [(1R)-3-hydroxy-1-methylpropyl]-, 1,1-dimethylethyl ester (9CI)

167216-17-3

General procedure for the synthesis of tert-butyl (R)-(4-hydroxybutan-2-yl)carbamate from methyl (R)-N-Boc-3-aminobutyrate: To a solution of methyl (R)-3-((tert-butoxycarbonyl)amino)butyrate (3.0 g, 14.76 mmol) in tetrahydrofuran (THF) (50 mL) was slowly added lithium aluminum (0.728 g, 19.19 mmol) hydroxide (0.728 g, 19.19 mmol) at -78°C under nitrogen protection. Lithium aluminum hydride (0.728 g, 19.19 mmol) was added slowly at -78°C under nitrogen protection. The reaction mixture was stirred at this temperature for 1 hour. Subsequently, the reaction system was slowly warmed to 0°C and the reaction was quenched by dropwise addition of water (0.7 mL) and 15% NaOH aqueous solution (0.7 mL). After quenching, the mixture was stirred at room temperature for 1 h and then filtered through a diatomaceous earth pad. The filtrate was dried over anhydrous sodium sulfate and concentrated under reduced pressure to give tert-butyl (R)-(4-hydroxybutan-2-yl)carbamate (1.3 g).

[References]

[1] Advanced Synthesis and Catalysis, 2010, vol. 352, # 1, p. 92 - 96
[2] Patent: US2011/237814, 2011, A1. Location in patent: Page/Page column 11
[3] Patent: WO2014/114249, 2014, A1. Location in patent: Page/Page column 21
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