HuagongsheHuagongshe Chemistry Print Report · For research reference only
9-amino-3,4-dihydroacridin-1(2H)-one → HCID 13756059, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 9-amino-3,4-dihydroacridin-1(2H)-one | HCID 184361 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13756059 | HCID 13756059 | — |
Reaction Steps
In 100 ml of dry tetrahydrofuran was suspended 5.00 g of 9-amino-3,4-dihydroacridin-1(2H)-one at ice temperature and 78 ml (4 eq) of 1.2M CH3Li solution in ether was added thereto at such a rate as to avoid bubbling. The reaction mixture was stirred overnight as it warmed to ambient temperature. The next day 20 ml more of the CH3Li solution was added to drive the reaction to a completion. After 0.5 hour the reaction was quenched with excess water and 4.97 g of the precipitate was collected and air dried. The product was recrystallized from MeOH/toluene. The yield was 2.06 g (38%) of granules, melting point 250° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04754050 |
| Source dataset | uspto-grants-1988_06 |
| ORD ID | ord-2cab61b9849a4b9fa4abd9fed2e4cc35 |
| Source note | uspto-grants-1988_06 |