HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 22648244, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178507989 | HCID 178507989 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 22648244 | HCID 22648244 | — |
Reaction Steps
3-Aminoquinolin-4-ol (6 g) was refluxed with acetic anhydride (8 eq.) until analysis by thin layer chromatography indicated that the reaction was complete. The reaction mixture was cooled, diluted with ice and water, made basic with 10% sodium hydroxide and then extracted with dichloromethane. The extract was washed with water and brine, dried over magnesium sulfate and then concentrated under vacuum. The residue was purified by column chromatography (silica gel eluting with methanol/ethyl acetate) to provide 5.1 g of 2-methyloxazolo[4,5-c]quinoline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06809203B2 |
| Source dataset | uspto-grants-2004_10 |
| ORD ID | ord-5e15c382952d49d79d9c8e3880f89cae |
| Source note | uspto-grants-2004_10 |