Toluene → 3-[2-(4-Bromophenyl)thiazol-4-yl]butanenitrile

HRID 1701943Notes

Reaction equation

HRID 1701943 reaction equation
[Br:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([NH2:8])=[S:7])=[CH:4][CH:3]=1.ClC[C:13](=O)[CH2:14][CH2:15][CH2:16][C:17]#[N:18].[C:20]1(C)C=CC=CC=1>>[Br:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]2[S:7][CH:13]=[C:14]([CH:15]([CH3:20])[CH2:16][C:17]#[N:18])[N:8]=2)=[CH:4][CH:3]=1

Participants

4

Reactant 3

HCID 1140TolueneHCID 15492894-BromothiobenzamideHCID 108206696-Chloro-5-oxohexanenitrile

Product 1

HCID 205047413-[2-(4-Bromophenyl)thiazol-4-yl]butanenitrile

Procedure

A mixture of 4-bromothiobenzamide (2.16 g., 0.01 mole) and 6-chloro-5-oxohexanenitrile (2.28 g., 0.012 mole) is heated at 60° C. in toluene for 12 hours. On cooling and partial evaporation, there is obtained 3-[2-(4-bromophenyl)thiazol-4-yl]butanenitrile.

Workup

  1. temperatureOn cooling
  2. custompartial evaporation

Sources & evidence

ORD record
ord-fc5d160973bc4a50acbbed30b87a2e9d
Source dataset
uspto-grants-1983_04
Patent number
US04379791

Reaction notes

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