Citric Acid → HCID 131712653, compound
Reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([CH3:7])[C:2]=1[CH3:8].CI.[OH-].[C:12]([OH:24])(=[O:23])[CH2:13][C:14]([CH2:19][C:20]([OH:22])=[O:21])([C:16]([OH:18])=[O:17])[OH:15]>>[C:12]([O-:24])(=[O:23])[CH2:13][C:14]([CH2:19][C:20]([O-:22])=[O:21])([C:16]([O-:18])=[O:17])[OH:15].[CH3:12][N+:1]1[CH:6]=[CH:5][CH:4]=[C:3]([CH3:7])[C:2]=1[CH3:8].[CH3:12][N+:1]1[CH:6]=[CH:5][CH:4]=[C:3]([CH3:7])[C:2]=1[CH3:8].[CH3:12][N+:1]1[CH:6]=[CH:5][CH:4]=[C:3]([CH3:7])[C:2]=1[CH3:8]Participants
5
Procedure
2-3-Lutidine is reacted with methyl iodide; the halide intermediate is converted to the hydroxide with Rexyn 201, and then reacted with citric acid.
Sources & evidence
- ORD record
- ord-f17d9df8e80e47b98a1ca4d97312b7d5
- Source dataset
- uspto-grants-1982_01
- Patent number
- US04312367
Reaction notes
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