HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → 7-(Allyloxy)-4-methyl-2H-chromen-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Methylumbelliferone | HCID 5280567 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 7-(Allyloxy)-4-methyl-2H-chromen-2-one | HCID 238952 | 98.1% |
Reaction Steps
7-Hydroxy-4-methylcoumarin (70.00 g, 0.397 mol), anhydrous K2CO3 (140 g, 1.01 mol), and allyl bromide (100 ml, 1.15 mol) were added to 2.0 L of reagent grade acetone. The milky mixture was refluxed for sixteen hours with overhead stirring, allowed to cool to room temperature, and filtered. Solids were washed once with reagent grade acetone (150 ml.), the filtrate and wash combined, and the resulting combined filtrate concentrated to dryness with a rotary evaporator to obtain 7-allyloxy-4-methylcoumarin (84.2 g, 98% yield). The crude product melted at 100.0°-101.5° C. (lit. 1 101° C.), showed only one spot in TLC, and was used in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04294847 |
| Source dataset | uspto-grants-1981_10 |
| ORD ID | ord-a70b5fbf8043442ba20665c18fed52ef |
| Source note | uspto-grants-1981_10 |