HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 13207879, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Carbamic acid, ethyl ester | HCID 5641 | — |
| Reactant | HCID 21521530 | HCID 21521530 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 13207879 | HCID 13207879 | — |
Reaction Steps
A mixture of 3.9 g of 2-(1-adamantylmethyl-amino)-5-nitrobenzophenone, 6.4 g of ethyl carbamate and 0.45 g of anhydrous zinc chloride was heated at 170°- 180°C for 1 hour, and then, distillating off the produced ethanol, heating was continued at that temperature for additional 1 hour. After cooling, chloroform was added thereto and insoluble material was filtered off. The chloroform layer was washed with water and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure and the residual oil was chromatographed on silica gel using chloroform as eluting solvent to give 1-(1-adamantylmethyl)-4-phenyl-6-nitro-2(1H)-quinazolinone, m.p. 230°- 233°C, following recrystallization from a mixture of ethanol and chloroform.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03970654 |
| Source dataset | uspto-grants-1976_07 |
| ORD ID | ord-f3fc40424b9344b498fab6c9f66a366d |
| Source note | uspto-grants-1976_07 |