5-BROMO-3-METHYL-BENZENE-1,2-DIAMINE
5-BROMO-3-METHYL-BENZENE-1,2-DIAMINE Basic information
- Product Name:
- 5-BROMO-3-METHYL-BENZENE-1,2-DIAMINE
- Synonyms:
-
- 5-BROMO-3-METHYL-BENZENE-1,2-DIAMINE
- 5-BROMO-3-METHYL-1,2-BENZENEDIAMINE
- 5-Bromo-3-methyl-1,2-diaminobenzene
- 1,2-Benzenediamine, 5-bromo-3-methyl-
- 3-methyl-5-bromo-o-phenylenediamine
- CAS:
- 76153-06-5
- MF:
- C7H9BrN2
- MW:
- 201.06
- Product Categories:
-
- pharmacetical
- Mol File:
- 76153-06-5.mol
5-BROMO-3-METHYL-BENZENE-1,2-DIAMINE Chemical Properties
- Melting point:
- 63 °C
- Boiling point:
- 298.8±35.0 °C(Predicted)
- Density
- 1.589±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2–8 °C
- pka
- 3.31±0.10(Predicted)
- Appearance
- Brown to dark brown Solid
- InChI
- InChI=1S/C7H9BrN2/c1-4-2-5(8)3-6(9)7(4)10/h2-3H,9-10H2,1H3
- InChIKey
- UOFSLKHZOPVGHG-UHFFFAOYSA-N
- SMILES
- C1(N)=CC(Br)=CC(C)=C1N
- CAS DataBase Reference
- 76153-06-5
5-BROMO-3-METHYL-BENZENE-1,2-DIAMINE Usage And Synthesis
Uses
5-Bromo-3-methylbenzene-1,2-diamine is used as an intermediate in organic synthesis.
Synthesis
77811-44-0
76153-06-5
Step 1: Stannous chloride (SnCl2, 5.0 g, 26.1 mmol) was added to an ethanol (EtOH, 20 mL) suspension of 4-bromo-2-methyl-6-nitroaniline (2.0 g, 8.7 mmol). The reaction mixture was heated to reflux for 14 h, followed by cooling to room temperature and vacuum concentration. The residue was diluted with ethyl acetate (EtOAc, 100 mL) and partitioned between saturated aqueous sodium bicarbonate (NaHCO3) solution (200 mL) and water. The resulting slurry was filtered through a Celite pad and the wet filter cake was washed with ethyl acetate (3 x 50 mL). The filtrate was washed sequentially with saturated aqueous sodium bicarbonate, water, and brine, dried over anhydrous magnesium sulfate (MgSO4), filtered, and concentrated in vacuum to give 1.27 g (72% yield) of 5-bromo-3-methylbenzene-1,2-diamine (72) as a yellow oil: mass spectrum (ESI) m/z = 201.1 [M + 1]+.
References
[1] Patent: WO2013/26914, 2013, A1. Location in patent: Page/Page column 130
[2] Bioorganic and Medicinal Chemistry Letters, 2007, vol. 17, # 11, p. 3072 - 3076
[3] Patent: US2005/54655, 2005, A1. Location in patent: Page/Page column 15-16
[4] Patent: US2004/44203, 2004, A1. Location in patent: Page 28
[5] Chemische Berichte, 1884, vol. 17, p. 776
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