HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl bromide → 5-Acetoxy-12-acetyl-12H-benzo[a]phenothiazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl bromide | HCID 10482 | — |
| Reactant | 5-acetoxy-12H-benzo[a]phenothiazine | HCID 13712479 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 5-Acetoxy-12-acetyl-12H-benzo[a]phenothiazine | HCID 13712493 | — |
Reaction Steps
To a mixture of 5-acetoxy-12H-benzo[a]phenothiazine (3.0 g) and powdered 4 Angstrom molecular sieves (7.5 g) in 1,2-dichloroethane (75 ml) there was added slowly acetyl bromide (1.05 ml). The mixture was stirred at room temperature for 1 hour, then filtered. The filtrate was evaporated down to an oil which was triturated with a mixture of ether and hexane to afford solid title product (3 g), m.p. 141°-142° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04611056 |
| Source dataset | uspto-grants-1986_09 |
| ORD ID | ord-b48d170671494ee3a84e468131b036c9 |
| Source note | uspto-grants-1986_09 |