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Tert-Butyl 4-(bromomethyl)phenylcarbamate

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Tert-Butyl 4-(bromomethyl)phenylcarbamate Basic information

Product Name:
Tert-Butyl 4-(bromomethyl)phenylcarbamate
Synonyms:
  • Carbamic acid, [4-(bromomethyl)phenyl]-, 1,1-dimethylethyl ester
  • TERT-BUTYL 4-(BROMOMETHYL)PHENYLCARBAMATE
  • Carbamic acid, N-[4-(bromomethyl)phenyl]-, 1,1-dimethylethyl ester
  • 4-(1,1-dimethylethoxycarbonylamino)benzylbromide
  • tert-Butyl (4-(bromomethyl)
  • tert-butyl N-[4-(bromomethyl)phenyl]carbamate
  • N-Boc-4-(broMoMethyl)aniline
  • Carbamic acid, [4-(bromomethyl)phenyl]-, 1,1-dimethylethyl e...
CAS:
239074-27-2
MF:
C12H16BrNO2
MW:
286.16
Mol File:
239074-27-2.mol
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Tert-Butyl 4-(bromomethyl)phenylcarbamate Chemical Properties

Boiling point:
309.7±25.0 °C(Predicted)
Density 
1.376±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
13.49±0.70(Predicted)
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Safety Information

HS Code 
2921490090
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Tert-Butyl 4-(bromomethyl)phenylcarbamate Usage And Synthesis

Synthesis

To a 1 L round bottom flask was added (4-hydroxymethyl-phenyl)-carbamic acid tert-butyl ester (22.3 g, 0.10 mol) obtained from Examples 2pp through 2ooo, Step 1, dichloromethane (400 mL) and triphenylphospine (31.5 g, 0.12 mol). Upon cooling to 0 °C, N-bromosuccinimide (19.6 g, 0.11 mmol) was added in small portions, and the reaction was allowed to warm to room temperature and stirred under nitrogen for 1 h. The mixture was transferred into a large flask, and hexanes were added until the solution became turbid. The solution was eluted through a plug of silica (300 g) with 1:9 ethyl acetate: hexanes and concentrated to yield Tert-Butyl 4-(bromomethyl)phenylcarbamate (12.8 g, 0.057 mol, 57 percent) as a white solid.

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