3,5-Bis(2-cyanoprop-2-yl)benzyl bromide
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
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)
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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3,5-Bis(2-cyanoprop-2-yl)benzyl bromide(120511-84-4)Related Product Information
- Benzyl alcohol
- Sodium bromate
- 3'-(Trifluoromethyl)acetophenone
- Ethidium bromide
- Benzyl isocyanate
- Methyl 4-(bromomethyl)benzoate
- 4-BROMO-2,2-DIPHENYLBUTYRONITRILE
- BROMOPENTAMETHYLBENZENE
- Benzyl chloride
- Benzyl bromide
- Allyl bromide
- 2'-Methylacetophenone
- 4'-Bromoacetophenone
- Benzyl nicotinate
- Benzyl benzoate
- p-Nitrophenylacetonitrile
- 2-Bromoacetophenone
- Diphenylacetonitrile