Formaldehyde → HCID 21555876, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8](=[O:22])[C:9]1[CH:14]=[C:13]([Cl:15])[CH:12]=[CH:11][C:10]=1[N:16]1[C:20]([CH3:21])=[CH:19][N:18]=[CH:17]1.[CH2:23]=[O:24]>>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8](=[O:22])[C:9]1[CH:14]=[C:13]([Cl:15])[CH:12]=[CH:11][C:10]=1[N:16]1[C:20]([CH3:21])=[CH:19][N:18]=[C:17]1[CH2:23][OH:24]Participants
3
Procedure
In the manner given in Example 1, 2',5 -dichloro-2-(5-methylimidazol-1-yl)benzophenone is heated in a bomb to 150° C. with 37% aqueous formaldehyde solution to give 2',5-dichloro-2-[2-(hydroxymethyl)-5-methylimidazol-1-yl]benzophenone.
Sources & evidence
- ORD record
- ord-e91620bd89e946f98f7108fccfdfa79e
- Source dataset
- uspto-grants-1976_03
- Patent number
- US03941803
Reaction notes
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