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5-BROMO-3-METHYL-BENZENE-1,2-DIAMINE

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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
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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
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Safety Information

HazardClass 
IRRITANT
HS Code 
2921599090
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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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