2-amino-5-ethylphenol

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: To a solution of 2-nitro-5-ethylphenol(1 g, 6.4 mmol) in methanol(250 mL) was added 10% Pd/C (100 mg). The mixture was flushed with argon, then hydrogen was bubbled through the solution for 10 min. and a hydrogen atmosphere was maintained at balloon pressure overnight. The mixture was filtered through celite and the celite was washed with methanol. The solvent was evaporated and chromatography of the resulting solid on silica gel (5% MeOH/CH2Cl2) gave the desired product(750 mg, 91%). 1H NMR (CD3OD): d 6.41-6.17 (m, 3H). The mixture was flushed with argon hydrogen was bubbled through the solution for 10 min. a hydrogen atmosphere was maintained at balloon pressure overnight The mixture was filtered through celite the celite was washed with methanol The solvent was evaporated

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: To a solution of 2-nitro-5-ethylphenol(1 g, 6.4 mmol) in methanol(250 mL) was added 10% Pd/C (100 mg). The mixture was flushed with argon, then hydrogen was bubbled through the solution for 10 min. and a hydrogen atmosphere was maintained at balloon pressure overnight. The mixture was filtered through celite and the celite was washed with methanol. The solvent was evaporated and chromatography of the resulting solid on silica gel (5% MeOH/CH2Cl2) gave the desired product(750 mg, 91%). 1H NMR (CD3OD): d 6.41-6.17 (m, 3H). The mixture was flushed with argon hydrogen was bubbled through the solution for 10 min. a hydrogen atmosphere was maintained at balloon pressure overnight The mixture was filtered through celite the celite was washed with methanol The solvent was evaporated

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: To a solution of 2-nitro-5-ethylphenol(1 g, 6.4 mmol) in methanol(250 mL) was added 10% Pd/C (100 mg). The mixture was flushed with argon, then hydrogen was bubbled through the solution for 10 min. and a hydrogen atmosphere was maintained at balloon pressure overnight. The mixture was filtered through celite and the celite was washed with methanol. The solvent was evaporated and chromatography of the resulting solid on silica gel (5% MeOH/CH2Cl2) gave the desired product(750 mg, 91%). 1H NMR (CD3OD): d 6.41-6.17 (m, 3H). The mixture was flushed with argon hydrogen was bubbled through the solution for 10 min. a hydrogen atmosphere was maintained at balloon pressure overnight The mixture was filtered through celite the celite was washed with methanol The solvent was evaporated

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: To a solution of 2-nitro-5-ethylphenol (1 g, 6.4 mmol) in methanol (250 mL) was added 10% Pd/C (100 mg). The mixture was flushed with argon, then hydrogen was bubbled through the solution for 10 min. and a hydrogen atmosphere was maintained at balloon pressure overnight. The mixture was filtered through celite and the celite was washed with methanol. The solvent was evaporated and chromatography of the resulting solid on silica gel (5%MeOH/CH2CH2) gave the desired product (750 mg, 91 %). 1H NMR (CD3OD): d 6.41-6.17 (m, 3H). The mixture was flushed with argon hydrogen was bubbled through the solution for 10 min. a hydrogen atmosphere was maintained at balloon pressure overnight The mixture was filtered through celite the celite was washed with methanol The solvent was evaporated

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: To a solution of 2-nitro-5-ethylphenol(1 g, 6.4 mmol) in methanol(250 mL) was added 10% Pd/C (100 mg). The mixture was flushed with argon, then hydrogen was bubbled through the solution for 10 min. and a hydrogen atmosphere was maintained at balloon pressure overnight. The mixture was filtered through celite and the celite was washed with methanol. The solvent was evaporated and chromatography of the resulting solid on silica gel (5% MeOH/CH2Cl2) gave the desired product(750 mg, 91%). 1H NMR (CD3OD): d 6.41-6.17 (m, 3H). The mixture was flushed with argon hydrogen was bubbled through the solution for 10 min. a hydrogen atmosphere was maintained at balloon pressure overnight The mixture was filtered through celite the celite was washed with methanol The solvent was evaporated