HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 3-methyl-4-(methoxyphenyl)-5-phenyl-2(5H)-furanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Dicyclohexyl(2,4,6-trimethoxyphenyl)phosphine | HCID 46867875 | — |
| Reactant | Methoxyphenyl boronic acid | HCID 53405446 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-methyl-4-(methoxyphenyl)-5-phenyl-2(5H)-furanone | HCID 68153752 | 100% |
Reaction Steps
This reaction is carried out in the same manner as the reaction in example 4. The difference is that 3-methyl-4-chloride-5-phenyl-2(5H)— furanone (42.0 mg, 0.2 mmol), methoxyphenyl boronic acid (46.5 mg, 97%, 0.3 mmol), palladium acetate (2.3 mg, 0.01 mmol), dicyclohexyl(2,4,6-trimethoxyphenyl)phosphine (7.3 mg, 0.02 mmol), potassium carbonate (82.3 mg, 0.6 mmol) are reacted in 1 mL of toluene at 110° C. for 35 minutes and 3-methyl-4-(methoxyphenyl)-5-phenyl-2(5H)— furanone is obtained. The yield is 100%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09006491B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-27019d8a6598491fba6b665cb0cda4d5 |
| Source note | uspto-grants-2015_04 |