HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 15044008, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 178507165 | HCID 178507165 | — |
| Product | HCID 15044008 | HCID 15044008 | 52% |
Reaction Steps
A solution of 9-amino-3,4-dihydroacridin-1(2H)-one N-oxide (5.4 g) and acetic anhydride (60 ml) was heated to reflux and then concentrated. The residue was stirred in saturated sodium bicarbonate solution for one hr. The mixture was filtered and the filter cake was washed with water and dried under vacuum at 40° C. for three hrs to yield 1.93 g of product, mp 208° C. (dec). An additional 1.38 g, mp 208° C. (dec), of product was obtained by extraction of the tiltrate with ethyl acetate, evaporation of ethyl acetate extract, and trituration of the residue with diethyl ether; total 52% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05382594 |
| Source dataset | uspto-grants-1995_01 |
| ORD ID | ord-3e17ab538baa4ea69a93a016a295dfb3 |
| Source note | uspto-grants-1995_01 |