ChemicalBook--->CAS DataBase List--->292606-35-0

292606-35-0

292606-35-0 Structure

292606-35-0 Structure
IdentificationMore
[Name]

1-BOC-AMINO-2,2-DIMETHYL-1,3-PROPANEDIAMINE
[CAS]

292606-35-0
[Synonyms]

1-BOC-AMINO-2,2-DIMETHYL-1,3-PROPANEDIAMINE
BOC-1-AMINO-2,2-DIMETHYL-1,3-PROPYLDIAMINE
Carbamic acid, (3-amino-2,2-dimethylpropyl)-, 1,1-dimethylethyl ester (9CI)
(3-Amino-2,2-dimethylpropyl)carbamic Acid tert-Butyl Ester
N-(tert-Butoxycarbonyl)-2,2-dimethyl-1,3-propanediamine
N-Boc-2,2-dimethyl-1,3-propanediamine
tert-Butyl (3-Amino-2,2-dimethylpropyl)carbamate
[Molecular Formula]

C10H22N2O2
[MDL Number]

MFCD01076212
[Molecular Weight]

202.29
[MOL File]

292606-35-0.mol
Chemical PropertiesBack Directory
[Melting point ]

74 °C
[Boiling point ]

293.8±23.0 °C(Predicted)
[density ]

0.964±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C, protect from light
[form ]

powder to crystal
[pka]

12.86±0.46(Predicted)
[color ]

White to Almost white
[CAS DataBase Reference]

292606-35-0(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
[Hazard Codes ]

Xn
[Risk Statements ]

22
[HS Code ]

2924.19.8000
Spectrum DetailBack Directory
[Spectrum Detail]

1-BOC-AMINO-2,2-DIMETHYL-1,3-PROPANEDIAMINE(292606-35-0)1HNMR
Well-known Reagent Company Product InformationBack Directory
[TCI AMERICA]

N-(tert-Butoxycarbonyl)-2,2-dimethyl-1,3-propanediamine,>98.0%(GC)(T)(292606-35-0)
Hazard InformationBack Directory
[Synthesis]

2,2-DIMETHYL-1,3-PROPANEDIAMINE

7328-91-8

Di-tert-butyl dicarbonate

24424-99-5

1-BOC-AMINO-2,2-DIMETHYL-1,3-PROPANEDIAMINE

292606-35-0

Di-tert-butyl dicarbonate was slowly added to a solution of 2,2-dimethylpropane-1,3-diamine in dichloromethane (DCM) (500 mL) of 2,2-dimethylpropane-1,3-diamine (80 g, 783 mmol) and di-tert-butyl dicarbonate (91 mL, 391 mmol) at 0 °C. The reaction mixture was stirred at ambient temperature for 12 hours. Subsequently, the reaction mixture was concentrated to remove the solvent. The crude product was purified by column chromatography (neutral alumina) using methanol: dichloromethane (1:9) as eluent to afford tert-butyl (3-amino-2,2-dimethylpropyl)carbamate (50 g, 247 mmol, 31.6% yield) as a white solid. The structure of the product was confirmed by 1H NMR (400 MHz, CDCl3): δ 0.85 (s, 6H), 1.44 (s, 9H), 2.35-2.52 (m, 2H), 3.00 (br d, J = 6.14Hz, 2H), 5.16 (br s, 1H).

[References]

[1] Patent: WO2018/109648, 2018, A1. Location in patent: Page/Page column 64
[2] Journal of Medicinal Chemistry, 1998, vol. 41, # 2, p. 236 - 246
[3] Patent: US2005/20623, 2005, A1. Location in patent: Page 116
[4] Patent: EP1550657, 2005, A1. Location in patent: Page/Page column 46
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