Hydrochloric Acid → HCID 19696143, compound
Reaction equation
C([NH:4][C:5]1[C:6]([N+:20]([O-:22])=[O:21])=[CH:7][C:8]([Br:19])=[C:9]2[C:14]=1[CH2:13][CH:12]([O:15]C(=O)C)[CH2:11][CH2:10]2)(=O)C.Cl>C(O)(=O)C>[NH2:4][C:5]1[C:6]([N+:20]([O-:22])=[O:21])=[CH:7][C:8]([Br:19])=[C:9]2[C:14]=1[CH2:13][CH:12]([OH:15])[CH2:11][CH2:10]2Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 90 °C
Procedure
A mixture of acetic acid 8-acetylamino-5-bromo-7-nitro-1,2,3,4-tetrahydronaphthalen-2-yl ester (2 g, 5.4 mmol), acetic acid (15 mL) and 6N HCl (30 mL) was stirred at 90° C. for 18 h. The solvent was removed by rotoevaporation to give the product (1.6 g) as an orange solid in quantitative yield.
Workup
- customThe solvent was removed by rotoevaporation
Sources & evidence
- ORD record
- ord-10602da88ced42069c5f5e0b2ab4d1dc
- Source dataset
- uspto-grants-1998_02
- Patent number
- US05721234
Reaction notes
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