ChemicalBook > Product Catalog > Organic Chemistry > Carboxylic acids and derivatives > Tert-Butyl 4-(bromomethyl)phenylcarbamate
Tert-Butyl 4-(bromomethyl)phenylcarbamate
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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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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