HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3-Chloro-5-methylaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Stannous Chloride | HCID 24479 | — |
| Reactant | 3-Chloro-5-nitrotoluene | HCID 297887 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Chloro-5-methylaniline | HCID 12475434 | 97.4% |
Reaction Steps
An ethanol solution (75 mL) containing 1-chloro-3-methyl-5-nitro-benzene (5.0 g, 29 mmol) are added with SnCl2.2 H2O (32.8 g, 146 mmol). The reaction mixture was reflux for 3.0 h. The solution was concentrated under vacuum, and the residue was re-dissolved in aqueous NaOH, filtered, and extracted with EtOAc. The organic layer was collected, washed with brine, dried over MgSO4, and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel to give 3-chloro-5-methyl-phenylamine (4.0 g) as light yellow solids in 97% yield: 1H NMR (500 MHz, CDCl3) δ 6.56 (s, 1 H), 6.48 (s, 1 H), 6.36 (s, 1 H), 3.66 (bs, 2 H), 2.23 (s, 3 H); ESI-MS: m/z 141.7 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08946268B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-6a9f968374094ba38433675e5c30f096 |
| Source note | uspto-grants-2015_02 |