Basic information Safety Supplier Related

3,5-Bis(2-cyanoprop-2-yl)benzyl bromide

Basic information Safety Supplier Related

3,5-Bis(2-cyanoprop-2-yl)benzyl bromide Basic information

Product Name:
3,5-Bis(2-cyanoprop-2-yl)benzyl bromide
Synonyms:
  • 5-(BROMOMETHYL)-A,A,A,A-TETRAMETHYL-1,3-BENZENEDIACETONITRILE
  • 5-BROMOMETHYL-A,A,A',A'-TETRAMETHYL-1,3-BENZENEDIACETONITRILE
  • 5-(BROMOMETHYL)-ALPHA,ALPHA,ALPHA,ALPHA-TETRAMETHYL-1,3-BENZENEDIACETONITRILE
  • 1,3-Benzenediacetonitrile, 5-(bromomethyl)-α,α,α',α'-tetramethyl-
  • Anastrozole EP Impurity C
  • 2-2'-[5-(Bromomethyl)benzene-1,3- diyl]bis(2-methylpropanenitrile)
  • 3,5-Bis(1-cyano-1-methylethyl)benzyl Bromide
  • Anastrozole USP Related Compound D
CAS:
120511-84-4
MF:
C15H17BrN2
MW:
305.21
EINECS:
601-717-7
Product Categories:
  • Methyl Halides
  • Phenyls & Phenyl-Het
  • Anastrazole
  • Aromatics
  • Impurities
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • Anastrozole
  • Intermediate of Anastrozole
Mol File:
120511-84-4.mol
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3,5-Bis(2-cyanoprop-2-yl)benzyl bromide Chemical Properties

Melting point:
98-100°C
Boiling point:
380.0±37.0 °C(Predicted)
Density 
1.276±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,2-8°C
solubility 
Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
form 
Solid
color 
White to Off-White
InChI
InChI=1S/C15H17BrN2/c1-14(2,9-17)12-5-11(8-16)6-13(7-12)15(3,4)10-18/h5-7H,8H2,1-4H3
InChIKey
IHXHGCDOJLOZML-UHFFFAOYSA-N
SMILES
C1(C(C)(C)C#N)=CC(CBr)=CC(C(C)(C)C#N)=C1
CAS DataBase Reference
120511-84-4(CAS DataBase Reference)
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3,5-Bis(2-cyanoprop-2-yl)benzyl bromide Usage And Synthesis

Chemical Properties

Off-White Solid

Uses

α,α,α’,α’-Tetramethyl-5-bromomethyl-1,3-benzenediacetonitrile (Anastrozole EP Impurity C) is an impurity of Anastrozole (A637425) (impurity D).

Synthesis

120511-72-0

120511-84-4

Using 5,α,α,α',α'-pentamethyl-1,3-benzenediacetonitrile as raw material, 3,5-bis(1-cyano-1-methylethyl)toluene (600 g, 2.65 mol) was obtained after step III. The product was mixed with N-bromosuccinimide (519 g, 2.916 mol) and benzoyl peroxide (17 g, 0.053 mol) in carbon tetrachloride (4.5 L) and the reaction was carried out at reflux for 2 to 2.5 hours. After completion of the reaction, the reaction mixture was cooled and filtered. The filtrate was concentrated to dryness at 40°C to 45°C. The resulting solid was dissolved in 2-propanol (2L) at 75°C to 80°C, followed by slow cooling to 10°C to 15°C and stirring at this temperature for 1 hour. The reaction mixture was further cooled to -5 °C to 0 °C and stirring was continued for 2 h, after which it was filtered and the filter cake was washed with pre-cooled 2-propanol (200 ml). The filter cake was subsequently washed with hexane and blotted dry. Finally, the filter cake was dried under vacuum at 40 °C to 45 °C to afford the target product 3,5-bis(1-cyano-1-methylethyl)benzyl bromide (700.2 g, 87.0% yield).

References

[1] Patent: US2006/189670, 2006, A1. Location in patent: Page/Page column 5; 7
[2] Patent: US2006/35950, 2006, A1. Location in patent: Page/Page column 3; 11
[3] Patent: CN103554041, 2016, B. Location in patent: Paragraph 0014-0016
[4] Patent: US2009/221837, 2009, A1. Location in patent: Page/Page column 4
[5] Patent: WO2007/39913, 2007, A1. Location in patent: Page/Page column 14

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