HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 9-Acetoxyxanthene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | HCID 21482819 | HCID 21482819 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 9-Acetoxyxanthene | HCID 12543454 | — |
Reaction Steps
To 15 g. of 9-(N-methylcarbamoyloxy)xanthene, suspended in 200 ml. of dry ether, is added 18 ml. of glacial acetic acid with stirring. After 1 hour, the lower acid layer is removed. The ether phase is then cooled, neutralized with cold aqueous sodium bicarbonate, dried over anhydrous magnesium sulfate and concentrated in vacuo. The residue is recrystallized from benzene-hexane to give 9-acetoxyxanthene, m.p. 109°-112° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03996364 |
| Source dataset | uspto-grants-1976_12 |
| ORD ID | ord-f33f7e9c792d4c819a5f6e7f715a8039 |
| Source note | uspto-grants-1976_12 |