HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Dioxane → Ketone, 3-furyl phenyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 3-Bromobenzaldehyde | HCID 76583 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | 2-(Tributylstannyl)furan | HCID 4393688 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ketone, 3-furyl phenyl | HCID 201640 | 86% |
Reaction Steps
EX-592A) To a dioxane (20 mL) solution of 3-bromobenzaldehyde (0.63 mL, 5.4 mmol) was added 2-(tributylstannyl)furan (1.89 mL, 6.00 mL) and Pd(PPh3)2Cl2 (0.21 g, 0.30 mmol). The mixture was heated to reflux under argon for 1.5 h. The cooled mixture was poured into a mixture of saturated KF and ethyl acetate and stirred 18 h. The slurry was filtered through celite. The organic layer was separated, washed with brine, dried (MgSO4) and evaporated to an oil. Purification by flash chromatography on silica gel eluting with 5% ethyl acetate in hexane gave 0.80 g (86%) of the desired 3-(2-furanyl)benzaldehyde product as an yellow oil which solidified upon standing. MS: m/z=173.1 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06710089B2 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-c7218a36617a4189acd66a0662a36453 |
| Source note | uspto-grants-2004_03 |