HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Bromo-o-toluidine → 2-Methyl-3-(methylthio)benzenamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Bromo-o-toluidine | HCID 123538 | — |
| Reactant | Sodium methanethiolate | HCID 4378561 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | 1-Methylpyrrolidine | HCID 8454 | — |
| Product | 2-Methyl-3-(methylthio)benzenamine | HCID 18408360 | — |
Reaction Steps
At 20° C., 4.3 g (61.81 mmol) of sodium thiomethoxide were added with stirring and ice-cooling to 10 g (53.75 mmol) of 3-bromo-2-methylaniline in 100 ml of N-methylpyrrolidine. After addition of 200 mg of copper powder, the reaction mixture was transferred into an autoclave and stirred at 240° C. for 16 h. The reaction solution was subsequently poured into 300 ml of ice-water and extracted 3× with methyl tert-butyl ether. The organic extracts were washed with water, dried and concentrated. The residue was chromatographed over silica gel using methylene chloride, giving 1.7 g (20.6% of theory) of the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06472349B1 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-f84650b5341e493aa73967b557cc91aa |
| Source note | uspto-grants-2002_10 |