Ammonium Hydroxide → 6-Amino-5-nitro-1-tetralone
Reaction equation
C([NH:4][C:5]1[C:6]([N+:16]([O-:18])=[O:17])=[C:7]2[C:12](=[CH:13][CH:14]=1)[C:11](=[O:15])[CH2:10][CH2:9][CH2:8]2)(=O)C.[OH-].[NH4+]>Cl>[NH2:4][C:5]1[C:6]([N+:16]([O-:18])=[O:17])=[C:7]2[C:12](=[CH:13][CH:14]=1)[C:11](=[O:15])[CH2:10][CH2:9][CH2:8]2Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The product from Example 81 (1 g) was treated with 6N hydrochloric acid (30 ml) at reflux for 2 hours and the reaction cooled then basified with ammonium hydroxide. The desired product was filtered, washed and dried.
Workup
- temperatureat reflux for 2 hours
- temperaturethe reaction cooled
- filtrationThe desired product was filtered
- washwashed
- customdried
Sources & evidence
- ORD record
- ord-6c32b94f6dd94432b0b222811c94b446
- Source dataset
- uspto-grants-1987_01
- Patent number
- US04634705
Reaction notes
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