HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Dioxane → 3-(2-Furanyl)4-(4-morpholinyl)benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | 2-(Tributylstannyl)furan | HCID 4393688 | — |
| Reactant | 3-Bromo-4-morpholinobenzaldehyde | HCID 23506020 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-(2-Furanyl)4-(4-morpholinyl)benzaldehyde | HCID 23506036 | 84% |
Reaction Steps
EX-604B) To a dioxane (8 mL) solution of the aldehyde from EX-604A (0.77 g, 2.8 mmol) was added 2-(tributylstannyl)furan (1.07 mL, 3.42 mmol) and Pd(PPh3)2Cl2 (0.12 g, 0.17 mmol). The mixture was heated to reflux under argon for 18 h. The cooled mixture was poured into a mixture of saturated aq. KF and ethyl acetate and stirred 3 h. The slurry was filtered through celite. The organic layer was separated, washed with brine, dried (MgSO4) and evaporated to a yellow oil. Purification by silica gel flash chromatography eluting with 20% ethyl acetate in hexane gave 0.61 g (84%) of the desired 3-(2-furanyl)4-(4-morpholinyl)benzaldehyde product as a yellow oil. MS: m/z=258.1 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06710089B2 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-00daf0f797e04c8594831611bfd26551 |
| Source note | uspto-grants-2004_03 |