HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexene → 7-hydroxy-3-(4-methoxyphenyl)-2H-1-benzopyran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexene | HCID 8079 | — |
| Reactant | 7-benzyloxy-3-(4-methoxyphenyl)-2H-1-benzopyran | HCID 59592104 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 7-hydroxy-3-(4-methoxyphenyl)-2H-1-benzopyran | HCID 9859847 | 94.9% |
Reaction Steps
Cyclohexene (1.5 mL) and Pd(OH)2/C (0.15 g) were added to a solution of compound 1 (0.3 g, 0.87 mmol) in ethanol (20 mL). The resultant mixture was stirred under a reflux temperature of 78° C. for 2 hrs, and then cooled to room temperature. After filtration, the filtrate was concentrated in vacuo, followed by purification via silica gel column chromatography (ethyl acetate/n-hexane=1:4), thus giving the title compound 3a as a colorless crystal (0.21 g, 94% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07875735B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-e419364d7b0c47459d06fad7341fe4f6 |
| Source note | uspto-grants-2011_01 |