Imidazole → HCID 18976102, compound

HRID 2393503Notes

Reaction equation

HRID 2393503 reaction equation
[CH:1]1[C:13]2[CH2:12][C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[C:5]=2[CH:4]=[CH:3][C:2]=1[CH:14](O)[C:15]1[CH:20]=[CH:19][CH:18]=[C:17]([Cl:21])[CH:16]=1.[NH:23]1[CH:27]=[CH:26][N:25]=[CH:24]1>>[Cl:21][C:17]1[CH:16]=[C:15]([CH:20]=[CH:19][CH:18]=1)[CH:14]([N:23]1[CH:27]=[CH:26][N:25]=[CH:24]1)[C:2]1[CH:3]=[CH:4][C:5]2[C:6]3[C:11](=[CH:10][CH:9]=[CH:8][CH:7]=3)[CH2:12][C:13]=2[CH:1]=1

Participants

3

Reactant 2

HCID 795ImidazoleHCID 54066918HCID 54066918, compound

Product 1

HCID 18976102HCID 18976102, compound

Procedure

Using α-(9H-fluoren-2-yl)-3-chlorobenzyl alcohol and imidazole as starting compounds, the process of Example 1 was repeated to obtain 1-[3-chloro-α-(9H-fluoren-2-yl)benzyl]-1H-imidazole.

Sources & evidence

ORD record
ord-3d6ba88c2fea41668fa633c9de0fb10a
Source dataset
uspto-grants-1998_09
Patent number
US05807880

Reaction notes

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