Ethanol → HCID 86738573, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[C:12]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)=[CH:11][N:10]([CH2:19][CH2:20][CH2:21][CH2:22][CH2:23]CC(O)=O)[C:9]2=[O:28])=[CH:4][CH:3]=1.[OH-:29].[Na+].[CH2:31]([OH:33])[CH3:32]>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([N:8]2[C:12]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)=[CH:11][N:10]([CH:19]([CH2:20][CH2:21][CH2:22][CH3:23])[CH2:32][C:31]([OH:29])=[O:33])[C:9]2=[O:28])=[CH:6][CH:7]=1Participants
4
Procedure
The product is produced as described in example 18 from 13.5 g of 7-[3-(4-chlorophenyl)-2-oxo-4-phenyl-4-imidazolin-1-yl] enanthic acid ethel ester, 1.28 g of NaOH in 60 cc. of ethanol.
Workup
- customThe product is produced
Sources & evidence
- ORD record
- ord-2d11956633804233a74b61c785b38fbd
- Source dataset
- uspto-grants-1982_09
- Patent number
- US04349684
Reaction notes
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