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180976-09-4

180976-09-4 Structure

180976-09-4 Structure
IdentificationBack Directory
[Name]

2-(N-BOC-METHYLAMINO)ACETONITRILE
[CAS]

180976-09-4
[Synonyms]

JACS-180976-09-4
2-[Boc(methyl)amino]acetonitrile
N-Boc-2-(methylamino)acetonitrile
2-(N-BOC-METHYLAMINO)ACETONITRILE
2-(N-Boc-N-MethylaMino)-acetonitrile
tert-Butyl (cyanomethyl)(methyl)carbamate
CYANOMETHYL-METHYL-CARBAMIC ACID TERT-BUTYL ESTER
N-(cyanomethyl)-N-methylcarbamic acid tert-butyl ester
Carbamic acid, N-(cyanomethyl)-N-methyl-, 1,1-dimethylethyl ester
[Molecular Formula]

C8H14N2O2
[MDL Number]

MFCD06658361
[MOL File]

180976-09-4.mol
[Molecular Weight]

170.21
Chemical PropertiesBack Directory
[Boiling point ]

244.5±19.0 °C(Predicted)
[density ]

1.033±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

-1.91±0.70(Predicted)
[Appearance]

Light brown to yellow Liquid
[InChI]

InChI=1S/C8H14N2O2/c1-8(2,3)12-7(11)10(4)6-5-9/h6H2,1-4H3
[InChIKey]

AXNPHDXTYKKHSJ-UHFFFAOYSA-N
[SMILES]

C(OC(C)(C)C)(=O)N(CC#N)C
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2926907090
Spectrum DetailBack Directory
[Spectrum Detail]

2-(N-BOC-METHYLAMINO)ACETONITRILE(180976-09-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

Di-tert-butyl dicarbonate

24424-99-5

Methylaminoacetonitrile hydrochloride

25808-30-4

2-(N-BOC-METHYLAMINO)ACETONITRILE

180976-09-4

GENERAL STEPS: To a dichloromethane (DCM, 100 mL) suspension of 2-methylaminoacetonitrile hydrochloride (11.45 g, 107.4 mmol) was added triethylamine (31.5 mL, 226 mmol), followed by the slow addition of di-tert-butyl dicarbonate (22.3 g, 102.2 mmol). The reaction mixture was stirred at room temperature overnight. After completion of the reaction, the mixture was filtered to remove insoluble salts and the filtrate was concentrated under reduced pressure. The crude product was purified by silica gel column chromatography using a 10-20% ethyl acetate/cyclohexane gradient elution. Fractions containing the target product were collected, combined and concentrated under reduced pressure to give tert-butyl (cyanomethyl)(methyl)carbamate (11.94 g, 69% yield) as a colorless liquid.LC-MS (Method 5): retention time 2.82 min, [M + H]+ m/z 171.1.

[References]

[1] Journal of Medicinal Chemistry, 1996, vol. 39, # 16, p. 3070 - 3088
[2] Patent: WO2008/23157, 2008, A1. Location in patent: Page/Page column 115
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