HuagongsheHuagongshe Chemistry Print Report · For research reference only
7-Methoxy-4-methyl-2H-1-benzopyran → 2,3-Dihydro-7-methoxy-4-methyl-4H-1-benzopyran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7-Methoxy-4-methyl-2H-1-benzopyran | HCID 12209412 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2,3-Dihydro-7-methoxy-4-methyl-4H-1-benzopyran | HCID 13497018 | 99.6% |
Reaction Steps
The alkene mixture of step (b) (29 g) was dissolved in ethanol (300 ml) and hydrogenated in the presence of 5% palladium on charcoal (1.0 g) at 45 psi; until hydrogen uptake had ceased. The catalyst was filtered off through a supercel filter aid and the filtrate was evaporated to give the desired compound 29.2 g (99.4%). NMR and MS analysis were correct for the required compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04159273 |
| Source dataset | uspto-grants-1979_06 |
| ORD ID | ord-52de91b2cbf04d3094d9998fed630a42 |
| Source note | uspto-grants-1979_06 |