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4-Bromo-2,6-dimethylaniline

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4-Bromo-2,6-dimethylaniline manufacturers

4-Bromo-2,6-dimethylaniline Basic information
Product Name:4-Bromo-2,6-dimethylaniline
Synonyms:TIMTEC-BB SBB002410;2,6-Dimethyl-4-bromoaniline;2,6-Xylidine, 4-bromo-;2-Amino-5-bromo-m-xylene, 4-Bromo-2,6-xylidine;4-BroMo-2,6-diMethylaniline, 97+%;4 - broMine - 2, 6 - diMethylaniline;Benzenamine, 4-bromo-2,6-dimethyl-;4-bromo-2,6-dimethylaniline,98%
CAS:24596-19-8
MF:C8H10BrN
MW:200.08
EINECS:246-337-9
Product Categories:Anilines, Amides & Amines;Bromine Compounds;Benzenes;Aniline;Aromatic Halides (substituted);bc0001
Mol File:24596-19-8.mol
4-Bromo-2,6-dimethylaniline Structure
4-Bromo-2,6-dimethylaniline Chemical Properties
Melting point 48-51 °C (lit.)
Boiling point 120°C 0,2mm
density 1.4423 (rough estimate)
refractive index 1.5748 (estimate)
Fp >230 °F
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility Chloroform, Methanol
pka3.60±0.10(Predicted)
form Liquid
color Clear yellow to orange to amber
BRN 1936300
InChIInChI=1S/C8H10BrN/c1-5-3-7(9)4-6(2)8(5)10/h3-4H,10H2,1-2H3
InChIKeyQGLAYJCJLHNIGJ-UHFFFAOYSA-N
SMILESC1(N)=C(C)C=C(Br)C=C1C
CAS DataBase Reference24596-19-8(CAS DataBase Reference)
NIST Chemistry ReferenceBenzenamine, 4-bromo-2,6-dimethyl-(24596-19-8)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 38-43-36/37/38-20/21/22
Safety Statements 36/37-36/37/39-26
RIDADR UN2811/6.1/III
WGK Germany 3
F 8-10-23
Hazard Note Harmful
HazardClass 6.1
HS Code 29214990
Storage Class6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard ClassificationsAcute Tox. 3 Dermal
Acute Tox. 3 Inhalation
Acute Tox. 4 Oral
Aquatic Acute 1
Aquatic Chronic 1
Carc. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
4-Bromo-2,6-xylidine English
SigmaAldrich English
ACROS English
ALFA English
4-Bromo-2,6-dimethylaniline Usage And Synthesis
Chemical Propertiesbrown crystals
Uses4-Bromo-2,6-dimethylaniline has been used in the preparation of:
  • 4-bromo-N-(1-(6-(1-isopropyl-1H-benzo[d]imidazol-2-yl)pyridin-2-yl)ethylidene)-2,6-dimethylbenzenamine
  • N-(4-Bromo-2,6-dimethylphenyl)-5-trimethylammoniumsalicylaldimine chloride
  • ethynyl-functionalized persistent perylene diimide-multichromophore
Reactions 4-Bromo-2,6-dimethylaniline has been shown to react with acid solutions to form hydrogen bromide gas and ammonium chloride crystals.
Synthesis
2,6-Dimethylaniline

87-62-7

4-Bromo-2,6-dimethylaniline

24596-19-8

The general procedure for the synthesis of 4-bromo-2,6-dimethylaniline from 2,6-dimethylaniline was as follows: 1-methoxy-3,5-dimethylbenzene (100 mg, 0.73 mmol), N-bromosuccinimide (NBS, 260 mg, 1.46 mmol), and a stainless steel ball (5 mm in diameter) were placed in a 10 mL stainless steel grinding jar. The ball milling reaction was carried out and the reaction process was monitored by thin layer chromatography (TLC) and proton nuclear magnetic resonance (1H NMR). Upon completion of the reaction, the reaction mixture was transferred to 30 mL of ethyl acetate and cooled at 0°C. The filtrate (containing product) and precipitate (spent succinimide) were obtained by filtration through filter paper and separated. The filtrate was concentrated under vacuum to give 250 mg (85% yield) of 4-bromo-2,6-dimethylaniline (2b) as a colorless powder. To test the efficiency of the large-scale reaction, monobromination was carried out under the same conditions using 1.3 g of 1-methoxy-3,5-dimethylbenzene for 1 h. The product was isolated in 87% yield. During the reaction, the grinding equipment was suspended and a small amount of sample was removed from the reaction tank for TLC and 1H NMR analysis, after which the reaction was continued, and the time of this operation was not included in the total reaction time.

References[1] Tetrahedron Letters, 2005, vol. 46, # 51, p. 8959 - 8963
[2] Tetrahedron Letters, 2009, vol. 50, # 9, p. 1007 - 1009
[3] Synthetic Communications, 2010, vol. 40, # 5, p. 647 - 653
[4] Synthetic Communications, 2009, vol. 39, # 23, p. 4212 - 4220
[5] Journal fuer Praktische Chemie (Leipzig), 1988, vol. 330, # 2, p. 161 - 174
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