3-Bromo-4-methylbenzonitrile

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3-Bromo-4-methylbenzonitrile manufacturers

3-Bromo-4-methylbenzonitrile Basic information
Product Name:3-Bromo-4-methylbenzonitrile
Synonyms:3-BROMO-4-METHYLBENZONITRILE 97;3-Bromo-4-methylbenzonitrile 98%;3-Bromo-4-methylbenzonitrile;4-methyl-3-bromobenzonitrile;Benzonitrile, 3-bromo-4-methyl-;Bromo-4-methyl-benzonitrile;2-Bromo-4-cyanotoluene, 3-Bromo-p-tolunitrile
CAS:42872-74-2
MF:C8H6BrN
MW:196.04
EINECS:
Product Categories:cyanide| alkyl bromide;Miscellaneous;Bromine Compounds;Nitriles;C8 to C9;Cyanides/Nitriles;Nitrogen Compounds;Fluorobenzene
Mol File:42872-74-2.mol
3-Bromo-4-methylbenzonitrile Structure
3-Bromo-4-methylbenzonitrile Chemical Properties
Melting point 41-45 °C (lit.)
Boiling point 259.1±20.0 °C(Predicted)
density 1.51±0.1 g/cm3(Predicted)
Fp >230 °F
storage temp. Sealed in dry,Room Temperature
form fused solid
AppearanceWhite to off-white Solid
Water Solubility Insoluble in water.
InChIInChI=1S/C8H6BrN/c1-6-2-3-7(5-10)4-8(6)9/h2-4H,1H3
InChIKeyVXUMRYMTYKDWMO-UHFFFAOYSA-N
SMILESC(#N)C1=CC=C(C)C(Br)=C1
CAS DataBase Reference42872-74-2(CAS DataBase Reference)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 20/21/22
Safety Statements 36
RIDADR UN3439
WGK Germany 3
Hazard Note Harmful
HazardClass 6.1
PackingGroup III
HS Code 2926907090
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Dermal
Acute Tox. 4 Inhalation
Acute Tox. 4 Oral
MSDS Information
3-Bromo-4-methylbenzonitrile Usage And Synthesis
Chemical PropertiesOff-white crystalline
UsesUsed as pharmaceutical intermediate.
Synthesis
p-Tolunitrile

104-85-8

3-Bromo-4-methylbenzonitrile

42872-74-2

General procedure for the synthesis of 3-bromo-4-methylbenzonitrile from 4-methylbenzonitrile: 4-methylbenzonitrile (168 g, 1.46 mol) was dissolved in a mixed solution of H2SO4/H2O (800 mL, 1:1, v/v/v) at 10 °C and N-bromosuccinimide (NBS, 256 g, 1.43 mol) was added slowly. The reaction mixture was stirred under light-avoiding conditions for 48 hours. After completion of the reaction, the mixture was filtered and the filter cake was collected. The filter cake was dissolved in ethyl acetate (1000 mL) and the organic layer was washed sequentially with water and saturated saline. Subsequently, it was neutralized with NaOH solution to pH=7 and washed again with saturated saline. The organic layer was dried over anhydrous Na2SO4 and concentrated under reduced pressure to give 3-bromo-4-methylbenzonitrile (276.5 g, 89% yield) as a yellow solid.

References[1] Journal of Organic Chemistry USSR (English Translation), 1988, vol. 24, # 2, p. 217 - 223
[2] Zhurnal Organicheskoi Khimii, 1988, vol. 24, # 2, p. 248 - 255
[3] Patent: WO2011/22337, 2011, A1. Location in patent: Page/Page column 103-104
[4] Synlett, 2007, # 14, p. 2179 - 2184
[5] Organic Letters, 2006, vol. 8, # 4, p. 645 - 647
3-Bromo-4-methylbenzonitrile Preparation Products And Raw materials
Raw materialsp-Tolunitrile-->N-Bromosuccinimide-->Sulfuric acid
Tag:3-Bromo-4-methylbenzonitrile(42872-74-2) Related Product Information
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