HuagongsheHuagongshe Chemistry Print Report · For research reference only
7-Acetoxy-3-(3,4-dimethoxyphenyl)chromen-4-one → HCID 59263550, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7-Acetoxy-3-(3,4-dimethoxyphenyl)chromen-4-one | HCID 907985 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 59263550 | HCID 59263550 | 100% |
Reaction Steps
In a similar manner to Example 4.1, 7-acetoxy-3-(3,4-dimethoxyphenyl)chromen-4-one (1.4 g) and 5% Pd—C (0.24 g) were suspended in absolute ethanol (200 mL) and hydrogen was introduced to the system for 55 h until the reaction was complete. Filtration and evaporation gave a cis- and trans-mixture of 7-acetoxy-3-(3,4-dimethoxyphenyl)chroman-4-ol (1.4 g, 100%). This mixture was used in the next step without any further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07700644B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-ba5ea009fbeb4731833ff17ef1fee237 |
| Source note | uspto-grants-2010_04 |