HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,8-Diazabicyclo(5.4.0)undec-7-ene → 4H-Pyrano(2,3-b)pyridine, 6-bromo-2-(3,4-dichlorophenyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 6-Bromo-2-(3,4-dichlorophenyl)-2H-pyrano[2,3-b]pyridine | HCID 514909 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4H-Pyrano(2,3-b)pyridine, 6-bromo-2-(3,4-dichlorophenyl)- | HCID 514910 | — |
Reaction Steps
To a solution of 2.9 g of 6-bromo-2-(3,4-dichlorophenyl)-2H-pyrano[2,3-b]pyridine in 40 ml of tetrahydrofuran was added 0.5 ml of 1,8-diazabicyclo[5.4.0]undec-7-ene. After 1 hour at 25° C., the reaction mixture was partitioned between ethyl acetate and aqueous saturated ammonium chloride solution. The ethyl acetate layer was dried over magnesium sulfate and the solvent was evaporated to leave a solid residue. This was recrystallized from ethanol to give 6-bromo-2-(3,4-dichlorophenyl)-4H-pyrano[2,3-b]pyridine melting at about 138°-139.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04588733 |
| Source dataset | uspto-grants-1986_05 |
| ORD ID | ord-eafa897dc1514dfeadaa3a24cf00cebe |
| Source note | uspto-grants-1986_05 |