HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(4-Morpholinophenyl)-1-phenylprop-2-yn-1-ol → 6-Morpholino-3-(4-morpholinophenyl)-3-phenyl-3h-naphtho[2,1-b]pyran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(4-Morpholinophenyl)-1-phenylprop-2-yn-1-ol | HCID 286741 | — |
| Reactant | 4-Morpholino-2-naphthol | HCID 10988042 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 6-Morpholino-3-(4-morpholinophenyl)-3-phenyl-3h-naphtho[2,1-b]pyran | HCID 9806148 | 73.2% |
Reaction Steps
A solution of 4-morpholino-2-naphthol (1.5 g, 6.5 mmol) and 1(4-morpholinophenyl)-1-phenylprop-2-yn-1-ol (1.92 g, 6.5 mmol) in toluene (65 cm3) containing acidic alumina (Brockmann 1), (4.0 g) was refluxed for 60 minutes. The cooled solution was filtered and the alumina was washed well with EtOAc (200 cm3). Removal of the solvent from the filtrate gave an oil which solidified on standing at room temperature. Recrystallisation from EtOAc/hexane gave 6-morpholino-3(4-morpholinophenyl)-3-phenyl-3H-naphtho[2,1-b]pyran (yield=2.4 g, theoretical yield=3.3 g 73%, m.p.=187-188° C. (uncorrected), λmax in toluene=469 nm, i.e. red-orange).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06294112B1 |
| Source dataset | uspto-grants-2001_09 |
| ORD ID | ord-fc326a65b57c4e238aec0b91b55f99a2 |
| Source note | uspto-grants-2001_09 |