HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 3-acetoxy-10-acetyl-4-chloro-10H-phenothiazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 3-acetoxy-4-chloro-10H-phenothiazine | HCID 13882026 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-acetoxy-10-acetyl-4-chloro-10H-phenothiazine | HCID 13882032 | — |
Reaction Steps
To 1.1 g of 3-acetoxy-4-chloro-10H-phenothiazine (see Example 4) was added acetyl chloride (7 ml), DMF (5 ml) and potassium tert-butoxide (0.42 g). The reaction mixture was stirred at ambient temperature for 1 hour and then, poured in water. The resulting precipitate was filtered and purified by chromatography on silica gel to give (1.08 g) 3-acetoxy-10-acetyl-4-chloro-10H-phenothiazine (m.p. 155° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04666907 |
| Source dataset | uspto-grants-1987_05 |
| ORD ID | ord-c9c006496aa34893a501b9f853e62abb |
| Source note | uspto-grants-1987_05 |