Hydrochloric Acid → HCID 28401656, compound
Reaction equation
Cl.[Br:2][C:3]1[CH:4]=[CH:5][C:6]([O:13][CH:14]2[CH2:18][CH2:17][CH2:16][CH2:15]2)=[C:7]([NH:9]C(=O)C)[CH:8]=1.[OH-].[Na+]>C(O)C>[Br:2][C:3]1[CH:4]=[CH:5][C:6]([O:13][CH:14]2[CH2:18][CH2:17][CH2:16][CH2:15]2)=[C:7]([CH:8]=1)[NH2:9]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Concentrated hydrochloric acid (5.8 ml) was added to an ethanol solution (100 ml) of N-(5-bromo-2-cyclopentyloxyphenyl)acetamide (3.4 g, 11.4 mmol), and the resulting mixture was stirred for 3 hours while heating under reflux. After the reaction mixture was cooled to room temperature, a 5N sodium hydroxide solution (14.2 ml) was added to obtain a pH of 11. The resulting mixture was then extracted with dichloromethane. The organic layer was washed with a saturated sodium chloride aqueous solution, and then concentrated under reduced pressure. The residue was then purified by silica gel column chromatography (n-hexane:ethyl acetate=4:1). The purified product was concentrated under reduced pressure to thereby obtain 2.97 g of oily pale yellow 5-bromo-2-cyclopentyloxyaniline (yield: 100%).
Workup
- temperaturewhile heating
- temperatureunder reflux
- customto obtain a pH of 11
- extractionThe resulting mixture was then extracted with dichloromethane
- washThe organic layer was washed with a saturated sodium chloride aqueous solution
- concentrationconcentrated under reduced pressure
- customThe residue was then purified by silica gel column chromatography (n-hexane:ethyl acetate=4:1)
- concentrationThe purified product was concentrated under reduced pressure
Sources & evidence
- ORD record
- ord-8b0bac5b2b54496692e47ac38604cc81
- Source dataset
- uspto-grants-2016_08
- Patent number
- US09403773B2
Reaction notes
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