4-(2-Bromoethyl)benzonitrile

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4-(2-Bromoethyl)benzonitrile Basic information
Product Name:4-(2-Bromoethyl)benzonitrile
Synonyms:4-(2-Bromoethyl)benzonitrile;4-Cyanophenethyl bromide;p-(2-Bromoethyl)benzonitrile;p-Cyanophenethyl bromide;Benzonitrile, 4-(2-bromoethyl)-
CAS:72054-56-9
MF:C9H8BrN
MW:210.07
EINECS:
Product Categories:
Mol File:72054-56-9.mol
4-(2-Bromoethyl)benzonitrile Structure
4-(2-Bromoethyl)benzonitrile Chemical Properties
Melting point 53-54℃
Boiling point 290℃
density 1.43
Fp 129℃
storage temp. Sealed in dry,Room Temperature
form solid
AppearanceWhite to off-white Solid
InChI1S/C9H8BrN/c10-6-5-8-1-3-9(7-11)4-2-8/h1-4H,5-6H2
InChIKeyNNNRGWOWXNCGCV-UHFFFAOYSA-N
SMILESBrCCC1=CC=C(C#N)C=C1
Safety Information
HS Code 2926907090
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
MSDS Information
4-(2-Bromoethyl)benzonitrile Usage And Synthesis
Synthesis
4-(2-HYDROXYETHYL)BENZONITRILE

69395-13-7

4-(2-Bromoethyl)benzonitrile

72054-56-9

General procedure for the synthesis of 4-(2-bromoethyl)benzonitrile from 4-(2-hydroxyethyl)benzonitrile: to a stirred solution of 4-(2-hydroxyethyl)benzonitrile (1.0 g, 6.8 mmol, 1.0 eq.) in dichloromethane (DCM, 20 mL) was added sequentially carbon tetrabromide (CBr4, 4.5016 g, 13.6 mmol, 2.0 eq.) and triphenylphosphine (TPP, 3.835 g, 13.6 mmol, 2.0 equiv). The reaction mixture was stirred at room temperature for 5 hours and the progress of the reaction was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the reaction mixture was diluted with water and extracted with ethyl acetate (EtOAc). The organic layers were combined, dried with anhydrous sodium sulfate, filtered and the filtrate was concentrated. The crude product was purified by column chromatography to afford pure 4-(2-bromoethyl)benzonitrile (1.3 g, 91% yield). The results of liquid chromatography-mass spectrometry (LC-MS, Method 23): retention time (Rt) = 2.01 min; mass-to-charge ratio (m/z) = 210.05 ([M+H]+).

References[1] Patent: WO2018/149986, 2018, A1. Location in patent: Page/Page column 95
[2] Pharmazie, 1982, vol. 37, # 1, p. 13 - 16
[3] ACS Medicinal Chemistry Letters, 2014, vol. 5, # 1, p. 65 - 68
[4] Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1979, p. 1128 - 1132
[5] Patent: US5811459, 1998, A
4-(2-Bromoethyl)benzonitrile Preparation Products And Raw materials
Raw materialsBenzaldehyde, 4-(2-bromoethyl)--->4-(2-Hydroxyethyl)benzonitrile-->Triphenylphosphine-->Carbon tetrabromide-->Dichloromethane
Preparation Products4-(2-Amino-ethyl)-benzoic acid
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