Benzoyl Peroxide → 4'-(Bromomethyl)-2-cyanobiphenyl

HRID 1368963Notes

Reaction equation

HRID 1368963 reaction equation
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=2[C:14]#[N:15])=[CH:4][CH:3]=1.[Br:16]N1C(=O)CCC1=O.C(OOC(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1>C(Cl)(Cl)(Cl)Cl>[Br:16][CH2:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=2[C:14]#[N:15])=[CH:6][CH:7]=1

Participants

5

Reactant 3

HCID 7187Benzoyl PeroxideHCID 67184N-bromobutanimideHCID 1455122-Cyano-4'-methylbiphenyl

Product 1

HCID 15019124'-(Bromomethyl)-2-cyanobiphenyl

Reagents, catalysts & solvents 1

HCID 5943Carbon TetrachlorideSolvent

Procedure

A solution of 5.59 g of 4′-methyl-2-cyanobiphenyl, 29 immol of N-bromosuccinimide, 9 mmol of benzoylperoxide and 500 mL of carbontetrachloride was refluxed for 3 hours. After cooling to room temperature, the resulting suspension was filtered and then concentrated in vacuo to provide the crude 4′-bromornethyl-2-cyanobiphenyl. The product was recrystallized from ether to yield 4.7 g of product; mp. 114.5°-120.0°. NMR (200 MHz, CDCl3)δ 7.82-7.37 (m, 8H); 4.50 (s, 2H). Anal. Calcd. for C14H10BrN: C, 61.79, H, 3.70; N, 5.15. Found: C, 62.15; H, 3.45; N, 4.98.

Workup

  1. filtrationthe resulting suspension was filtered
  2. concentrationconcentrated in vacuo
  3. customto provide the crude 4′-bromornethyl-2-cyanobiphenyl
  4. customThe product was recrystallized from ether

Sources & evidence

ORD record
ord-242fcaebf9a14730bdc785ecb3ec1f6d
Source dataset
uspto-grants-2003_06
Patent number
US06576652B2

Reaction notes

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