ChemicalBook--->CAS DataBase List--->113778-69-1

113778-69-1

113778-69-1 Structure

113778-69-1 Structure
IdentificationBack Directory
[Name]

N-Methoxy-N,2-dimethylpropanamide
[CAS]

113778-69-1
[Synonyms]

N-Methoxy-N-MethylisobutyraMide
N-Methoxy-N,2-dimethylpropanamide
Propanamide, N-methoxy-N,2-dimethyl-
N-METHOXY-N,2-DIMETHYLPROPANAMIDE(WX619185)
[Molecular Formula]

C6H13NO2
[MDL Number]

MFCD11847606
[MOL File]

113778-69-1.mol
[Molecular Weight]

131.17
Chemical PropertiesBack Directory
[Boiling point ]

137.7±23.0 °C(Predicted)
[density ]

0.945±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

Chloroform, DCM, Ethyl Acetate
[form ]

Oil
[color ]

Colourless
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H319-H335-H302+H312+H332-H315
[Precautionary statements ]

P280-P301+P312-P362+P364
[HS Code ]

2928009090
Hazard InformationBack Directory
[Uses]

N-Methoxy-N-methylisobutyramide is an intermediate in the synthesis of pteridine derivatives with potential protective effects with vibrio cholerae infection.
[Synthesis]

N,O-Dimethylhydroxylamine hydrochloride

6638-79-5

Isobutyryl chloride

79-30-1

N-Methoxy-N,2-dimethylpropanamide

113778-69-1

I. Synthesis of N-methoxy-N,2-dimethylpropionamide. Isobutyryl chloride (6.02 mL, 57.5 mmol) was added slowly and dropwise to a solution of N,O-dimethylhydroxylamine hydrochloride (5.61 g, 57.5 mmol) and triethylamine (17.6 mL, 126.5 mmol) in dichloromethane (100 mL). The reaction mixture was stirred at room temperature overnight. After completion of the reaction, the reaction mixture was washed with deionized water (100 mL) and the organic layer was dried with anhydrous magnesium sulfate. The solvent was removed by concentration under reduced pressure and the crude product was purified by silica gel column chromatography (eluent: n-hexane to 9:1 n-hexane/ethyl acetate) to afford N-methoxy-N,2-dimethylpropanamide (5.55 g, 74% yield).1H NMR (300 MHz, DMSO-d6) δ 3.72 (s, 3H), 3.31 (m, 1H), 3.18 (s, 3H) 1.09 (d, J = 6.87 Hz, 6H).

[References]

[1] Organic Letters, 2012, vol. 14, # 9, p. 2250 - 2253
[2] Journal of Medicinal Chemistry, 2015, vol. 58, # 7, p. 3117 - 3130
[3] Journal of Medicinal Chemistry, 2017, vol. 60, # 12, p. 4840 - 4860
[4] Chemistry - A European Journal, 2017, vol. 23, # 57, p. 14345 - 14357
[5] Organic and Biomolecular Chemistry, 2013, vol. 11, # 20, p. 3337 - 3340
Spectrum DetailBack Directory
[Spectrum Detail]

N-Methoxy-N,2-dimethylpropanamide(113778-69-1)1HNMR
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