HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → HCID 178456711, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone | HCID 6775 | — |
| Reactant | Propylamine | HCID 7852 | — |
| Reactant | 5-Hydroxy-12H-benzo[a]phenothiazine-7,7-dioxide | HCID 13712480 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178456711 | HCID 178456711 | 62.8% |
Reaction Steps
To a suspension of 5-hydroxy-12H-benzo[a]phenothiazine-7,7-dioxide (594 mg) in THF (10 ml) was added 2,3-dichloro 5,6-dicyano-1,4-benzoquinone (1.021 gram). The mixture was stirred at room temperature for 2 minutes, then there was added n-propyl amine (0.2 ml). The stirring was continued for 0.5 hour, then the mixture was evaporated to dryness. To the residue was added 50 ml dichloromethane and the mixture was stirred for 15 minutes and filtered. The filtrate was evaporated to dryness and the residue crystallized from a mixture of toluene and hexane to afford the title compound (442 mg) as a red-brown crystalline solid, m.p. 149°-151° C. (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04667032 |
| Source dataset | uspto-grants-1987_05 |
| ORD ID | ord-4c457c88b89346088d00c22d419648ef |
| Source note | uspto-grants-1987_05 |