Nitric Acid → HCID 19989839, compound
Reaction equation
[Br:1][C:2]1[CH:14]=[CH:13][C:5]([C:6]([CH2:8][CH2:9][C:10]([OH:12])=[O:11])=[O:7])=[CH:4][CH:3]=1.[N+:15]([O-])([OH:17])=[O:16]>>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([C:6]([CH2:8][CH2:9][C:10]([OH:12])=[O:11])=[O:7])=[CH:13][C:14]=1[N+:15]([O-:17])=[O:16]Participants
3
Conditions
- Temperature
- -5 °C
Procedure
Under salt-ice cooling, 3-(4-bromobenzoyl)propionic acid (75.0 g, 291.7 mmol) was added to fuming nitric acid (200 mL) in portions at such a rate that the temperature of the reaction solution could be maintained at −5° C. or lower. After stirring at −12° C. to −10° C. for 1 hour, the reaction solution was poured onto ice. The solid which precipitated was collected by filtration, washed with purified water, and thereafter dried under reduced pressure to obtain 3-(4-bromo-3-nitrobenzoyl)propionic acid (91.0 g).
Workup
- additionthe reaction solution was poured onto ice
- customThe solid which precipitated
- filtrationwas collected by filtration
- washwashed with purified water
- customdried under reduced pressure
Sources & evidence
- ORD record
- ord-7cbf4d8a5c494dd7a268abfcd71562be
- Source dataset
- uspto-grants-2015_07
- Patent number
- US09072734B2
Reaction notes
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