Formaldehyde → HCID 21555847, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([N:16]2[C:20]([CH3:21])=[CH:19][N:18]=[CH:17]2)=[C:6]([CH:15]=1)[C:7]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)=[O:8].[CH2:22]=[O:23]>C1(C)C(C)=CC=CC=1>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([N:16]2[C:20]([CH3:21])=[CH:19][N:18]=[C:17]2[CH2:22][OH:23])=[C:6]([CH:15]=1)[C:7]([C:9]1[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=1)=[O:8]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
In the manner given in Example 1, 2.96 g. of 5-chloro-2-(5-methylimidazol-1-yl)benzophenone is heated in a bomb with paraformaldehyde in xylene to 140° C. to give 5-chloro-2-[5-methyl-2-(hydroxymethyl)imidazol-1-yl]benzophenone.
Sources & evidence
- ORD record
- ord-c9d05f263bfe4a07998af0f121a8cc6b
- Source dataset
- uspto-grants-1976_03
- Patent number
- US03941803
Reaction notes
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