Basic information Safety Supplier Related

TERT-BUTYL 4-(BROMOMETHYL)BENZYLCARBAMATE

Basic information Safety Supplier Related

TERT-BUTYL 4-(BROMOMETHYL)BENZYLCARBAMATE Basic information

Product Name:
TERT-BUTYL 4-(BROMOMETHYL)BENZYLCARBAMATE
Synonyms:
  • TERT-BUTYL 4-(BROMOMETHYL)BENZYLCARBAMATE
  • 4-(BroMoMethyl)benzylcarbaMate
  • N-BOC-4-(BROMOMETHYL)BENZYLAMINE
  • 4-(Boc-aMinoMethyl)benzylbroMide
  • (4-BroMoMethyl-benzyl)-carbaMic acid tert-butyl ester
  • Carbamic acid, N-[[4-(bromomethyl)phenyl]methyl]-, 1,1-dimethylethyl ester
  • tert-butyl N-[[4-(bromomethyl)phenyl]methyl]carbamate
  • benzyl 4-(bromomethyl)benzylcarbamate
CAS:
187283-17-6
MF:
C13H18BrNO2
MW:
300.19
Mol File:
187283-17-6.mol
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TERT-BUTYL 4-(BROMOMETHYL)BENZYLCARBAMATE Chemical Properties

storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
Appearance
White to light yellow Solid
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Safety Information

HS Code 
2921490090
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TERT-BUTYL 4-(BROMOMETHYL)BENZYLCARBAMATE Usage And Synthesis

Synthesis

123986-64-1

187283-17-6

General procedure for the synthesis of tert-butyl 4-(bromomethyl)benzylcarbamate from tert-butyl 4-(hydroxymethyl)benzylcarbamate: 4-(N-tert-butoxycarbonylaminomethyl)benzyl alcohol (250 mg, 1.1 mmol) was dissolved in tetrahydrofuran (5 mL) and cooled down to -78 °C. At this temperature, phosphorotriamine (30 μL, 0.32 mmol) was slowly added and the reaction lasted for 2 hours. Upon completion of the reaction, solid sodium bicarbonate (50 mg) was added to quench the reaction. The solid insoluble material was removed by filtration and the filtrate was subsequently evaporated to afford the target product 4-(tert-butoxycarbonylaminomethyl)benzyl bromide (300 mg, 95% yield).

References

[1] Patent: US6680311, 2004, B1. Location in patent: Page/Page column 151
[2] Journal of Medicinal Chemistry, 2009, vol. 52, # 1, p. 33 - 47
[3] Patent: WO2006/117549, 2006, A1. Location in patent: Page/Page column 155
[4] Chemical Science, 2017, vol. 8, # 12, p. 7947 - 7953

TERT-BUTYL 4-(BROMOMETHYL)BENZYLCARBAMATESupplier

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