Nitric Acid → HCID 19990451, compound
Reaction equation
[N+:1]([O-:4])(O)=[O:2].[C:5]([NH:12][C:13]1[CH:18]=[C:17]([Cl:19])[C:16]([Cl:20])=[C:15]([Cl:21])[CH:14]=1)([C:7]([O:9][CH2:10][CH3:11])=[O:8])=[O:6]>>[C:5]([NH:12][C:13]1[CH:14]=[C:15]([Cl:21])[C:16]([Cl:20])=[C:17]([Cl:19])[C:18]=1[N+:1]([O-:4])=[O:2])([C:7]([O:9][CH2:10][CH3:11])=[O:8])=[O:6]Participants
3
Conditions
- Temperature
- 0 °C
Procedure
20 ml 100% nitric acid was cooled to 0° C. and 2.0 g (6.8 mmol) N-ethoxalyl-3,4,5-trichloroaniline was added. The reaction mixture was stirred at 0° C. for 10 min. and 200 ml ice-water was added. The precipitate was filtered off, washed with water and ethanol to give 1.2 g (52%) of N-ethoxalyl-2-nitro-3,4,5-trichloroaniline. M.p. 84° C.
Workup
- filtrationThe precipitate was filtered off
- washwashed with water and ethanol
Sources & evidence
- ORD record
- ord-c97ee4613bf8426c937a9b2cfbb1b7cc
- Source dataset
- uspto-grants-1991_10
- Patent number
- US05061706
Reaction notes
Loading…