3-(4-Bromophenyl)propionitrile

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3-(4-Bromophenyl)propionitrile Basic information
Uses
Product Name:3-(4-Bromophenyl)propionitrile
Synonyms:3-(4-Bromophenyl)propionitrile 98%;3-(4-Bromophenyl)propanenitrile 98%;Benzenepropanenitrile, 4-broMo-;3-(4-Bromophenyl)propionitrile, 2-(4-Bromophenyl)ethyl cyanide;3-(4-Bromophenyl)propanenitrile98%;4-Bromobenzenepropanenitrile;3-(4-bromophenyl)propylnitrile;3-(4-Bromophenyl)propanenitrile
CAS:57775-08-3
MF:C9H8BrN
MW:210.07
EINECS:
Product Categories:
Mol File:57775-08-3.mol
3-(4-Bromophenyl)propionitrile Structure
3-(4-Bromophenyl)propionitrile Chemical Properties
Boiling point 118°C 1mm
density 1,42 g/cm3
storage temp. Sealed in dry,Room Temperature
Specific Gravity1.42
AppearanceWhite to off-white Solid
CAS DataBase Reference57775-08-3(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 20/21/22-36/37/38-52
Safety Statements 26-36/37/39
RIDADR 3276
Hazard Note Irritant
HazardClass IRRITANT, IRRITANT-HARMFUL
HS Code 2926907090
MSDS Information
3-(4-Bromophenyl)propionitrile Usage And Synthesis
Uses3-(4-bromophenyl)propionitrile is a nitrile compound that can be used as an intermediate in organic synthesis to prepare other heterocyclic compounds.
Synthesis
Diethyl cyanomethylphosphonate

2537-48-6

4-Bromobenzaldehyde

1122-91-4

3-(4-BROMOPHENYL)PROPIONITRILE

57775-08-3

General procedure for the synthesis of 3-(4-bromophenyl)propanenitrile from diethyl cyanomethylphosphonate and p-bromobenzaldehyde: (2) Prop-2-enenenitrile E/Z mixture of 3-(4-bromophenyl)pyridine (34.8 g, 0.63 L) was dissolved in methanol (0.21 L), and sodium borohydride (8.2 g) was slowly added at 0 °C under nitrogen protection. The reaction mixture was stirred at 100 °C for 1 hour. After completion of the reaction, the reaction solution was concentrated, water was added and the mixture was extracted with ethyl acetate. The organic layer was washed sequentially with water and saturated saline, dried over anhydrous magnesium sulfate, filtered and the solvent was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent ratio: hexane:ethyl acetate=100:0→65:35) to give the yellow oily product 3-(4-bromophenyl)propionitrile (28.1 g).

References[1] Patent: JP2015/231988, 2015, A. Location in patent: Paragraph 0328; 0329
3-(4-Bromophenyl)propionitrile Preparation Products And Raw materials
Raw materialsDiethyl cyanomethylphosphonate-->4-Bromobenzaldehyde-->Sodium borohydride-->Methanol-->Potassium tert-butoxide-->Tetrahydrofuran
Tag:3-(4-Bromophenyl)propionitrile(57775-08-3) Related Product Information
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