HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron Trichloride → Kampferol-3,4'-dimethyl ether
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron Trichloride | HCID 25135 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 7-Benzyloxy-2-(3,4-dimethoxy-phenyl)-5-methoxy-chromen-4-one | HCID 19358579 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Kampferol-3,4'-dimethyl ether | HCID 5351234 | 64% |
Reaction Steps
7-benzyloxy-3',4',5-trimethoxy flavone (565 mg, 1.35 mmol) was dissolved in 17 mL of methylenechloride, and then 1M of boron trichloride (3.79 mL, 3 equivalents) was added at temperature of 0° C. Then the reaction mixture was stirred for 30 minutes. When aqueous sodium acetate solution (5 mL) was added to the resultant reaction mixture, the product was obtained as a yellow crystal. The product was triturated with hexane and filtered to give the titled product (271 mg, 64%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06025387 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-3c27b2358b4e4bbe8759bae99d3b12a1 |
| Source note | uspto-grants-2000_02 |