Basic information Safety Supplier Related

tert-Butyl but-3-yn-1-ylcarbamate

Basic information Safety Supplier Related

tert-Butyl but-3-yn-1-ylcarbamate Basic information

Product Name:
tert-Butyl but-3-yn-1-ylcarbamate
Synonyms:
  • Carbamic acid, 3-butynyl-, 1,1-dimethylethyl ester (9CI)
  • Tert-Butylbut-3-ynylcarbamate
  • CarbaMic acid, N-3-butyn-1-yl-, 1,1-diMethylethyl ester
  • But-3-ynyl-carbaMic acid tert-butyl ester
  • N-BOC-BUT-3YN-1-YLAMINE
  • tert-Butyl but-3-yn-1-ylcarbaMate
  • tert-butyl N-but-3-ynylcarbamate
  • Tert-Butyl But-3-Yn-1-Ylcarbamate(WXC01948)
CAS:
149990-27-2
MF:
C9H15NO2
MW:
169.22
Product Categories:
  • N-BOC
Mol File:
149990-27-2.mol
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tert-Butyl but-3-yn-1-ylcarbamate Chemical Properties

Boiling point:
250.5±23.0 °C(Predicted)
Density 
0.976±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
pka
12.11±0.46(Predicted)
Appearance
Colorless to light yellow Liquid
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Safety Information

HS Code 
2924297099
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tert-Butyl but-3-yn-1-ylcarbamate Usage And Synthesis

Synthesis

6089-09-4

75-65-0

149990-27-2

General procedure for the synthesis of N-Boc-butyn-4-amine from 4-pentynoic acid and tert-butanol: To a solution of 4-pentynoic acid (1.96 g, 20 mmol) in tert-butanol (6 mL) was added triethylamine (3 mL) at 0 °C, followed by the slow addition of diphenylphosphoryl azide (note: the reaction will start rapidly and may proceed violently after addition). The reaction mixture was heated to 85 °C and kept overnight under nitrogen protection. Upon completion of the reaction, the solvent was removed by vacuum concentration and the crude product was purified by silica gel column chromatography using dichloromethane as eluent to give N-Boc-butyn-4-amine as a white solid (1.81 g, 53% yield).

References

[1] Patent: WO2007/28131, 2007, A1. Location in patent: Page/Page column 49

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