HuagongsheHuagongshe Chemistry Print Report · For research reference only
Stannous chloride dihydrate → 3-Chloro-5-methylaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Stannous chloride dihydrate | HCID 61436 | — |
| 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) were mixed with SnCl2.2H2O (32.8 g, 146 mmol). The reaction mixture was refluxed 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(s), 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), 3.66 (s, 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 | US08999983B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-1791404cd9314ce89afb7c5561301ec3 |
| Source note | uspto-grants-2015_04 |