ChemicalBook--->CAS DataBase List--->66389-80-8

66389-80-8

66389-80-8 Structure

66389-80-8 Structure
IdentificationBack Directory
[Name]

TERT-BUTYL 4-CYANOBENZYLCARBAMATE
[CAS]

66389-80-8
[Synonyms]

N-Boc-4-cyanobenzylamine
4-BOC-AMINOMETHYL-BENZONITRILE
TERT-BUTYL 4-CYANOBENZYLCARBAMATE
tert-butyl N-[(4-cyanophenyl)methyl]carbamate
Carbamic acid, N-[(4-cyanophenyl)methyl]-, 1,1-dimethylethyl ester
[Molecular Formula]

C13H16N2O2
[MDL Number]

MFCD08436197
[MOL File]

66389-80-8.mol
[Molecular Weight]

232.28
Chemical PropertiesBack Directory
[Melting point ]

90-92 °C
[Boiling point ]

392.9±35.0 °C(Predicted)
[density ]

1.10±0.1 g/cm3(Predicted)
[storage temp. ]

2-8°C
[pka]

11.91±0.46(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P280-P305+P351+P338
Hazard InformationBack Directory
[Synthesis]

Di-tert-butyl dicarbonate

24424-99-5

4-(Aminomethyl)benzonitrile hydrochloride

15996-76-6

TERT-BUTYL 4-CYANOBENZYLCARBAMATE

66389-80-8

(1) To a solution of 4-(aminomethyl)benzonitrile hydrochloride (5.00 g, 29.7 mmol) in dichloromethane (167 mL) at 0 °C was added sodium carbonate (7.54 g, 71.2 mmol). Subsequently, di-tert-butyl dicarbonate (7.57 mL, 32.6 mmol) was slowly added. The reaction mixture was gradually warmed to room temperature and stirred overnight. Upon completion of the reaction, water was added to terminate the reaction and the product was extracted with ethyl acetate. The organic layer was washed sequentially with water and saturated sodium chloride solution and dried over anhydrous sodium sulfate. The solvent was removed by concentration under reduced pressure, and the resulting crude product was purified by silica gel (NH) column chromatography (eluent: n-hexane/ethyl acetate=1:1) to give tert-butyl 4-cyanobenzylcarbamate (6.48 g, 94% yield).

[References]

[1] Angewandte Chemie - International Edition, 2012, vol. 51, # 18, p. 4431 - 4434
[2] Chemistry - A European Journal, 2018, vol. 24, # 68, p. 18075 - 18081
[3] Patent: WO2017/18803, 2017, A1. Location in patent: Paragraph 1552; 1553; 1554
[4] Journal of the American Chemical Society, 2012, vol. 134, # 25, p. 10317 - 10320
[5] Angewandte Chemie - International Edition, 2016, vol. 55, # 2, p. 528 - 533
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