HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → HCID 13055167, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | HCID 20468881 | HCID 20468881 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13055167 | HCID 13055167 | — |
Reaction Steps
The solution of 5.4 g of 2-(o-bromomethylphenyl)-5-bromo-2'-fluorobenzophenone in 10 ml of ethanol is added slowly to the solution of 150 ml of saturated ethanolic ammonia while stirring at room temperature. After 2 days the mixture is evaporated, the residue taken up in methylene chloride and the solution washed with aqueous sodium carbonate. The organic layer is dried, evaporated and 5 g of the residue chromatographed on 50 g of silica gel, using first toluene, then toluene-diethyl ether (9:1) as the eluent. The later fraction is evaporated and the residue crystallized from hexane to yield the 9-bromo-7-(o-fluorophenyl)-5H-dibenz[c,e]azepine melting at 104°-105°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04356176 |
| Source dataset | uspto-grants-1982_10 |
| ORD ID | ord-53caaee7a476410db3f9160d13984f3a |
| Source note | uspto-grants-1982_10 |