4-broMo-5-Methylbenzene-1,2-diaMine

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Company Name: Shanghai Sunway Pharmaceutical Technology Co., Ltd  
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4-broMo-5-Methylbenzene-1,2-diaMine manufacturers

4-broMo-5-Methylbenzene-1,2-diaMine Basic information
Product Name:4-broMo-5-Methylbenzene-1,2-diaMine
Synonyms:1,2-BenzenediaMine, 4-broMo-5-Methyl-;4-Bromo-5-methyl-1,2-benzenediamine;4-broMo-5-Methylbenzene-1,2-diaMine
CAS:102169-44-8
MF:C7H9BrN2
MW:201.06
EINECS:
Product Categories:
Mol File:102169-44-8.mol
4-broMo-5-Methylbenzene-1,2-diaMine Structure
4-broMo-5-Methylbenzene-1,2-diaMine Chemical Properties
Boiling point 298.6±35.0 °C(Predicted)
density 1.589±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form solid
pka3.58±0.10(Predicted)
AppearanceLight yellow to brown Solid
InChI1S/C7H9BrN2/c1-4-2-6(9)7(10)3-5(4)8/h2-3H,9-10H2,1H3
InChIKeyBYYYESJDKPVYGB-UHFFFAOYSA-N
SMILESCc1cc(N)c(N)cc1Br
Safety Information
Hazard Codes Xn
Risk Statements 22
WGK Germany 3
HS Code 2921511990
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
MSDS Information
4-broMo-5-Methylbenzene-1,2-diaMine Usage And Synthesis
Synthesis
4-bromo-5-methyl-2-nitroaniline

827-32-7

4-broMo-5-Methylbenzene-1,2-diaMine

102169-44-8

General procedure for the synthesis of 4-bromo-5-methylbenzene-1,2-diamine from 4-bromo-5-methyl-2-nitroaniline: 4.00 g (17.312 mmol) of 4-bromo-5-methyl-2-nitroaniline was dissolved in 100 mL of ethanol, and 15.63 g (69.248 mmol) of stannic chloride (II) dihydrate was added. The reaction mixture was stirred at 70 °C overnight. After completion of the reaction, it was cooled to room temperature, diluted by adding an appropriate amount of water, and the pH was adjusted to a weak base with saturated aqueous sodium bicarbonate solution. Subsequently, it was extracted three times with ethyl acetate, the organic phases were combined and dried with anhydrous sodium sulfate. The dried organic phase was concentrated by rotary evaporation under reduced pressure to obtain the crude product. The crude product was dried under high vacuum to finally obtain 3.23 g (89% yield) of the target compound 4-bromo-5-methylbenzene-1,2-diamine. The product was analyzed by LC-MS (Method 1): retention time Rt = 1.07 min; mass spectrum (EIpos): m/z = 201 [M + H]+. 1H-NMR (400 MHz, DMSO-d6) data were as follows: δ [ppm] = 2.08 (s, 3H), 4.51 (s, 2H), 4.52 (s, 2H), 6.43 (s. 1H), 6.66 (s, 1H).

References[1] Patent: WO2010/20363, 2010, A1. Location in patent: Page/Page column 81-82
4-broMo-5-Methylbenzene-1,2-diaMine Preparation Products And Raw materials
Raw materials4-bromo-5-methyl-2-nitroaniline-->4-Methyl-2-nitroaniline-->Stannous chloride-->Ethanol
Preparation Products5-Bromo-6-methyl-1H-benzimidazole
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