HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 13298921, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 13298918 | HCID 13298918 | — |
| Reactant | HCID 178418247 | HCID 178418247 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13298921 | HCID 13298921 | 129.2% |
Reaction Steps
In such a manner a mixture of 6-methyl-7-hydroxy-8-allylcoumarin (VII) (6.3 g), anhydrous AcONa (1.5 g) and acetic anhydride (40 ml) was refluxed for 1 h. The reaction mixture was gently diluted with water (40 ml), refluxed for 10 min and then poured into H2O (300 ml) yielding a precipitate, which was collected by filtration and washed several times with H2O. The dried product was crystallized from MeOH yielding 6-methyl-7-acetoxy-8-allylcoumarin (X) (6.1 g; m.p. 110°-11° C.). ##STR15##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05179217 |
| Source dataset | uspto-grants-1993_01 |
| ORD ID | ord-1e4fe41bfce74b06983c9687fc415827 |
| Source note | uspto-grants-1993_01 |