Formaldehyde → HCID 13179829, compound

HRID 267429Notes

Reaction equation

HRID 267429 reaction equation
[N+:1]([C:4]1[CH:5]=[CH:6][C:7]([N:18]2[CH:22]=[CH:21][N:20]=[CH:19]2)=[C:8]([CH:17]=1)[C:9]([C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=[O:10])([O-:3])=[O:2].[CH2:23]=[O:24]>C1(C)C(C)=CC=CC=1>[N+:1]([C:4]1[CH:5]=[CH:6][C:7]([N:18]2[CH:22]=[CH:21][N:20]=[C:19]2[CH2:23][OH:24])=[C:8]([CH:17]=1)[C:9]([C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=1)=[O:10])([O-:3])=[O:2]

Participants

4

Reactant 2

HCID 712FormaldehydeHCID 12392116HCID 12392116, compound

Product 1

HCID 13179829HCID 13179829, compound

Reagents, catalysts & solvents 1

HCID 7237O-XyleneSolvent

Procedure

In the manner given in Example 1, 5-nitro-2-(imidazol-1-yl)benzophenone is heated in a bomb with paraformaldehyde in xylene to 140° C. to give 5-nitro-2-[2-(hydroxymethyl)imidazol-1-yl]benzophenone.

Sources & evidence

ORD record
ord-efba09bbae21404f8551b1d1746114c5
Source dataset
uspto-grants-1976_03
Patent number
US03941803

Reaction notes

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