Identification | Back Directory | [Name]
TERT-BUTYL 3-(BROMOMETHYL)PHENYLCARBAMATE | [CAS]
118684-32-5 | [Synonyms]
N-Boc-3-(bromomethyl)aniline Ter-Butyl-3-(bromomethyl)phenyl carbamate TERT-BUTYL 3-(BROMOMETHYL)PHENYLCARBAMATE 2-Methyl-2-propanyl [3-(bromomethyl)phenyl]carbamate Carbamic acid, N-[3-(bromomethyl)phenyl]-, 1,1-dimethylethyl ester | [Molecular Formula]
C12H16BrNO2 | [MDL Number]
MFCD11974927 | [MOL File]
118684-32-5.mol | [Molecular Weight]
286.16 |
Chemical Properties | Back Directory | [Melting point ]
122 °C | [Boiling point ]
309.0±25.0 °C(Predicted) | [density ]
1.376±0.06 g/cm3(Predicted) | [storage temp. ]
Inert atmosphere,Store in freezer, under -20°C | [form ]
solid | [pka]
13.58±0.70(Predicted) | [color ]
White to off white |
Hazard Information | Back Directory | [Synthesis]
At -20 °C, tert-butyl (3-(hydroxymethyl)phenylcarbamate (120 g, 484 mmol) was dissolved in tetrahydrofuran (50 mL) and triphenylphosphine (254 g, 967 mmol) and N-bromosuccinimide (103 g, 580 mmol) were added sequentially. The reaction mixture was stirred at this temperature for 3 hours. After completion of the reaction, the solvent was removed by distillation under reduced pressure. The crude product was purified by silica gel column chromatography with the eluent being petroleum ether: ethyl acetate (100:1, v/v) to afford tert-butyl 3-(bromomethyl)phenylcarbamate (125 g, 437 mmol, 90% yield) as a white solid. It was analyzed by liquid chromatography-mass spectrometry (LCMS, Method 1, Table 7) with a retention time (R t) of 2.10 min; mass spectrometry (MS) showed m/z = 230,232 [M-t-Bu + H+]. | [References]
[1] Patent: WO2017/210471, 2017, A1. Location in patent: Paragraph 001137; 001138 [2] Bioorganic and Medicinal Chemistry, 2000, vol. 8, # 1, p. 73 - 93 [3] ChemBioChem, 2010, vol. 11, # 18, p. 2517 - 2520 [4] Patent: US2008/21032, 2008, A1. Location in patent: Page/Page column 56 [5] Journal of Medicinal Chemistry, 1989, vol. 32, # 4, p. 811 - 826 |
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