HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Allyl-7-hydroxy-8-methoxycoumarin → 7-Acetoxy-6-allyl-8-methoxycoumarin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Allyl-7-hydroxy-8-methoxycoumarin | HCID 21814500 | — |
| Reactant | Acetic anhydride pyridine | HCID 22348678 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 7-Acetoxy-6-allyl-8-methoxycoumarin | HCID 21814501 | — |
Reaction Steps
A solution of 2.32g. (0.010 mole) of 6-allyl-7-hydroxy-8-methoxycoumarin in 8 ml. of chloroform was treated with 4.5 ml. of acetic anhydride/pyridine, 1:2. The reactants were stirred at 25° for 2.0 hours and then partitioned between 1N HCl/methylene chloride. The aqueous phase was further extracted with methylene chloride. The organic extracts were combined, dried over sodium sulfate, and evaporated to afford pure 7-acetoxy-6-allyl-8-methoxycoumarin as a white solid, mp 101°-102°. Recrystallization from ethanol afforded an analytical sample, mp 102°-103°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04130568 |
| Source dataset | uspto-grants-1978_12 |
| ORD ID | ord-35cc6a46e79b46c6b636d3fe1c0ddc5b |
| Source note | uspto-grants-1978_12 |