1-Cyclopropyl-4-nitronaphthalene → 4-Cyclopropylnaphthalen-1-amine
Reaction equation
[CH:1]1([C:4]2[C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[C:7]([N+:14]([O-])=O)=[CH:6][CH:5]=2)[CH2:3][CH2:2]1>C(O)C.[Pd]>[NH2:14][C:7]1[C:8]2[C:13](=[CH:12][CH:11]=[CH:10][CH:9]=2)[C:4]([CH:1]2[CH2:3][CH2:2]2)=[CH:5][CH:6]=1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of 1-cyclopropyl-4-nitro-naphthalene (5 g, 23 mmol) in ethanol (200 mL) was stirred under hydrogen in the presence of Pd/C (10% net, 1.8 g). The reaction mixture was shaken overnight, then filtered over celite. The solvent was evaporated, and the residue was purified by silica gel chromatography to yield 1-amino-4-cyclopropyl-naphthalene (3.1 g, 73%).
Workup
- filtrationfiltered over celite
- customThe solvent was evaporated
- customthe residue was purified by silica gel chromatography
Sources & evidence
- ORD record
- ord-f2af901572bd4c44934ee503cbc04f0d
- Source dataset
- uspto-grants-2011_08
- Patent number
- US08003681B2
Reaction notes
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