Water → HCID 4184921, compound
Reaction equation
[N+:1]([C:4]1[CH:10]=[C:9]([O:11][CH3:12])[CH:8]=[CH:7][C:5]=1[NH2:6])([O-:3])=[O:2].[C:13](Cl)(=[O:18])[CH2:14][CH2:15][CH2:16][CH3:17].O>N1C=CC=CC=1>[C:13]([NH:6][C:5]1[CH:7]=[CH:8][C:9]([O:11][CH3:12])=[CH:10][C:4]=1[N+:1]([O-:3])=[O:2])(=[O:18])[CH2:14][CH2:15][CH2:16][CH3:17]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 0 °C
Procedure
4.2 g (0.025 mol) of 2-nitro-4-methoxy-aniline are dissolved in 30 ml of pyridine, cooled to 0° C. and treated with 3.3 g (0.0275 mol) of valeryl chloride with stirring. After stirring for 1 hour at ambient temperature, the mixture is poured into iced water, the crystals are filtered off under suction and dried.
Workup
- stirringAfter stirring for 1 hour at ambient temperature
- filtrationthe crystals are filtered off under suction
- customdried
Sources & evidence
- ORD record
- ord-1c890ec182e64bada1bcec7e25b7e916
- Source dataset
- uspto-grants-1996_07
- Patent number
- US05541229
Reaction notes
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