HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → (2-amino-4-fluorophenyl)-N-(1-methylethyl)-methylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Isopropylamine | HCID 6363 | — |
| Reactant | 4-Fluoro-2-nitrobenzaldehyde | HCID 76226 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | (2-amino-4-fluorophenyl)-N-(1-methylethyl)-methylamine | HCID 17777166 | — |
Reaction Steps
To a solution of 4-fluoro-2-nitro benzaldehyde (3.76 g, 25 mmol) in dry MeOH (120 ml), was added isopropyl amine (2.1 ml, 25 mmol) and the mixture stirred for 2 hours at room temperature in Argon atmosphere. Then it was then transferred into a Parr bottle containing 5% Pd on charcoal (246 mg) under Argon and hydrogenated at 30 psi for 18 hours. The suspension was filtered over a celite pad, washed with MeOH and evaporated at reduced pressure to afford (2-amino-4-fluorophenyl)-N-(1-methylethyl)-methylamine as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05929072 |
| Source dataset | uspto-grants-1999_07 |
| ORD ID | ord-6c924382919a405cbb3d6a693f7e8699 |
| Source note | uspto-grants-1999_07 |