Acetyl chloride → HCID 54441192, compound
Reaction equation
[N+:1]([C:4]1[N:8]([CH2:9][CH2:10][OH:11])[C:7]([CH:12]=[CH:13][N:14]([CH3:16])[CH3:15])=[N:6][CH:5]=1)([O-:3])=[O:2].[C:17](Cl)(=[O:19])[CH3:18]>>[N+:1]([C:4]1[N:8]([CH2:9][CH2:10][O:11][C:17](=[O:19])[CH3:18])[C:7]([CH:12]=[CH:13][N:14]([CH3:15])[CH3:16])=[N:6][CH:5]=1)([O-:3])=[O:2]Participants
3
Procedure
2,26 g. (0.01 mole) of 5-nitro-1-(2-hydroxyethyl)-2-(2-dimethylaminovinyl)-imidazole and 0.79 g. (0.01 mole) of acetyl chloride were reacted as described in Example 11. After pouring the reaction mixture on ice water, it was extracted with chloroform and the chloroform solution evaporated. The crude red oil exhibited the characteristic UV maxima in methanol:
Workup
- additionAfter pouring the reaction mixture on ice water, it
- extractionwas extracted with chloroform
- customthe chloroform solution evaporated
Sources & evidence
- ORD record
- ord-1afb53654eb543b5b50816c1f7fc50b5
- Source dataset
- uspto-grants-1976_04
- Patent number
- US03952007
Reaction notes
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