HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 21478721, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Isoamyl Nitrite | HCID 8053 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | HCID 21478799 | HCID 21478799 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 21478721 | HCID 21478721 | 70.2% |
Reaction Steps
To a solution of isopropyl 5-benzyloxy-2-aminophenylactate (13.2 g) in benzene (140 ml) were added potassium acetate (4.33 g) and then acetic anhydride (13.5 g) and the mixture was heated under reflux for 20 minutes. A solution of isopentyl nitrite (7.76 g) in benzene (30 ml) was added dropwise over 5 minutes under reflux and then refluxing was continued for further 3 hours. After allowing to cool to room temperature, insolubles were filtered off with Celite and concentrated under reduced pressure. The resulting residue (16.9 g) was purified by a silica gel column chromatography (hexane:ethyl acetate=9:1-4:1) to give the title compound (10.9 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05684003 |
| Source dataset | uspto-grants-1997_11 |
| ORD ID | ord-0c4788772b7245fb9a6581769e132543 |
| Source note | uspto-grants-1997_11 |