HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 13298915, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2H-1-Benzopyran-2-one, 7-hydroxy-6-methyl- | HCID 5412913 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 13298915 | HCID 13298915 | — |
Reaction Steps
A mixture of 6-methyl-7-hydroxycoumarin (I) (14.5 g), anhydrous K2CO3 (5 g), allyl bromide (15 ml) and acetone (400 ml) was refluxed for 12 h under stirring. From the refluxed mixture the solid was filtered and washed several times with acetone. The acetonic solution and the pooled washings were concentrated to dryness and the residue crystallized from MeOH, yielding 6-methyl-7-allyloxycoumarin (IV) (11.4 g; m.p. 124°-5° C.). ##STR10##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05001147 |
| Source dataset | uspto-grants-1991_03 |
| ORD ID | ord-1ad8c1e128114636b8e0cdfb891a0a9c |
| Source note | uspto-grants-1991_03 |