HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Benzothiazole, 5,6-dimethoxy-2-methyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Sulfide | HCID 14804 | — |
| Reactant | 4-Bromo-5-nitroveratrole | HCID 170968 | — |
| Reactant | Sulfur | HCID 5362487 | — |
| Product | Benzothiazole, 5,6-dimethoxy-2-methyl- | HCID 112829 | — |
Reaction Steps
1-Bromo-4,5-dimethoxy-2-nitro-benzene (10 g) was suspended into ethanol (50 ml). To the reaction mixture was added the suspension of sodium sulfide (5 g) and sulfur (0.65 g) in ethanol (12 ml). The reaction mixture was refluxed 1.5 hour and then the resultant solid was filtered and washed with hot water and ethanol. The dry solid was slurried with acetic acid (60 ml) and acetanhydridi (35 ml). To the suspension was gradually added zinc (16.6 g) and the suspension was stirred at room temperature for 15 min before filtering off. The residue was evaporated to dryness. The product was purified by column chromatography using toluene-ethyl acetate-acetic acid 8:1:1 as the eluent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08318785B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-e2b8445e6e684076841356a2e6169893 |
| Source note | uspto-grants-2012_11 |