3-Bromoanisole → 3-(4-Phenyl-1H-imidazol-1-yl)phenol

HRID 1493955Notes

Reaction equation

HRID 1493955 reaction equation
[N:1]1([C:6]2[CH:7]=[C:8]([OH:12])[CH:9]=[CH:10][CH:11]=2)[CH:5]=[CH:4][N:3]=[CH:2]1.[C:13]1(C2N=CNC=2)[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.BrC1C=C(OC)C=CC=1>>[C:13]1([C:4]2[N:3]=[CH:2][N:1]([C:6]3[CH:7]=[C:8]([OH:12])[CH:9]=[CH:10][CH:11]=3)[CH:5]=2)[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1

Participants

4

Reactant 3

HCID 169713-BromoanisoleHCID 104645913-(1H-Imidazol-1-yl)phenolHCID 178418822HCID 178418822, compound

Product 1

HCID 127184433-(4-Phenyl-1H-imidazol-1-yl)phenolYield 57%

Procedure

Following the procedure for preparation of 3-(1H-imidazol-1-yl)phenol (preparation 7), 4-phenylimidazole (20 g, 0.138 mole) and 3-bromoanisole (32 ml, 0.25 mole) were reacted to give the title compound in 57% yield, mp 195°-197° C.

Workup

  1. customwere reacted

Sources & evidence

ORD record
ord-527304fd518e43ea806bf616536622c4
Source dataset
uspto-grants-1991_06
Patent number
US05025031

Reaction notes

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