ChemicalBook--->CAS DataBase List--->99207-32-6

99207-32-6

99207-32-6 Structure

99207-32-6 Structure
IdentificationBack Directory
[Name]

TERT-BUTYL 4-HYDROXYBUTYLMETHYLCARBAMATE
[CAS]

99207-32-6
[Synonyms]

4-[Boc(methyl)amino]-1-butanol
N-Boc-4-(methylamino)butan-1-ol
TERT-BUTYL 4-HYDROXYBUTYLMETHYLCARBAMATE
tert-butyl N-(4-hydroxybutyl)-N-methylcarbamate
4-(N-tert-Butyloxycarbonyl-N-methylamino)butanol
(4-Hydroxy-butyl)-Methyl-carbaMic acid tert-butyl ester
Carbamic acid, (4-hydroxybutyl)methyl-, 1,1-dimethylethyl ester
Carbamic acid, N-(4-hydroxybutyl)-N-methyl-, 1,1-dimethylethyl ester
[Molecular Formula]

C10H21NO3
[MDL Number]

MFCD09953073
[MOL File]

99207-32-6.mol
[Molecular Weight]

203.28
Chemical PropertiesBack Directory
[storage temp. ]

2-8°C
[Appearance]

Colorless to light yellow Liquid
Safety DataBack Directory
[Symbol(GHS) ]

Skull and Crossbones (GHS06)
GHS06
[Signal word ]

Danger
[Hazard statements ]

H301
[Precautionary statements ]

P301+P310
[HS Code ]

2924297099
Spectrum DetailBack Directory
[Spectrum Detail]

TERT-BUTYL 4-HYDROXYBUTYLMETHYLCARBAMATE(99207-32-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

4-METHYLAMINO BUTANOL

42042-68-2

Di-tert-butyl dicarbonate

24424-99-5

TERT-BUTYL 4-HYDROXYBUTYLMETHYLCARBAMATE

99207-32-6

General procedure for the synthesis of N-Boc-N-methyl-4-aminomethylbutanol from 4-(methylamino)butan-1-ol and di-tert-butyl dicarbonate: a solution of 4-(methylamino)butan-1-ol (2.76g, 26.8mmol) in triethylamine/methanol (1:7 v/v, 100mL) was stirred for 10 minutes at 0 °C. Subsequently, a solution of di-tert-butyl dicarbonate (8.76 g, 40.2 mmol) in methanol (20 mL) was added dropwise over 10 min. The reaction mixture was stirred under nitrogen protection for 1 hour. After that, the temperature of the reaction system was allowed to gradually increase to room temperature and stirring was continued overnight. Upon completion of the reaction, the solvent was removed by evaporation under reduced pressure and the residue was dissolved in dichloromethane and washed with deionized water. The organic layer was separated, dried with anhydrous sodium sulfate, filtered and concentrated to afford the colorless oily product N-Boc-N-methyl-4-aminomethylbutanol (4.54 g, 84% yield), which could be used in the next reaction without further purification.1H NMR (CDCl3) δ 3.66 (t, 2H), 3.23 (t, 2H), 2.83 (s, 3H), 1.78 (br s, 1H), 1.51-1.60 (m, 4H), 1.44 (s, 9H).

[References]

[1] Journal of Medicinal Chemistry, 2013, vol. 56, # 14, p. 5819 - 5828
[2] Patent: WO2013/148230, 2013, A1. Location in patent: Page/Page column 30
[3] Tetrahedron Letters, 2006, vol. 47, # 43, p. 7551 - 7556
[4] Patent: US4975439, 1990, A
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