HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 3,5-Dichloro-4-(napthalen-2-ylsulfanyl)-phenylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Stannous chloride dihydrate | HCID 61436 | — |
| Reactant | 2-(2,6-Dichloro-4-nitro-phenylsulfanyl)-napthalene | HCID 22148877 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3,5-Dichloro-4-(napthalen-2-ylsulfanyl)-phenylamine | HCID 22148834 | 84% |
Reaction Steps
To a 0.1M solution 2-(2,6-Dichloro-4-nitro-phenylsulfanyl)-napthalene (89) (774 mg, 2.2 mmol), in EtOAc was added tin(II)chloride dihydrate, obtained from Aldrich, (2.49 g, 11.05 mmol). The resulting mixture was refluxed for 2 hour. The crude reaction mixture was cooled to ambient temperature and excess 2M aqueous NaOH was added and allowed to stir for 15 minutes. Solid tin salts precipitated from the solution, were filtered off through a pad of celite and washed with EtOAc (200 mL). The organic layer was washed twice with brine (200 mL), dried over Na2SO4, and concentrated under vacuum to yield 592 mg (84%) of (90) which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06770648B2 |
| Source dataset | uspto-grants-2004_08 |
| ORD ID | ord-1787f6f2dd92451cb1d75b19e0954e94 |
| Source note | uspto-grants-2004_08 |