HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 2-ethoxy-7-nitro-5-phenyl-3H-1,4-benzodiazepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-(2-Azido-1-ethoxyethylideneamino)-5-nitrobenzophenone | HCID 20317263 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-ethoxy-7-nitro-5-phenyl-3H-1,4-benzodiazepine | HCID 20317264 | — |
Reaction Steps
To a solution of 2.5 parts of 2-(2-azido-1-ethoxyethylideneamino)-5-nitrobenzophenone produced in Step (2) in 30 parts by volume of benzene is added with stirring 1.78 parts of triphenylphosphine. The mixture is stirred for further 1.5 hours and the solvent is removed by distillation. The residue is extracted with a mixture of n-hexane and acetone (7:3), and the soluble fraction is purified by means of chromatography employing Silica Gel, whereupon 2-ethoxy-7-nitro-5-phenyl-3H-1,4-benzodiazepine is obtained as pale yellow crystals. Recrystallization from ether-n-hexane gives pale yellow prisms melting at 143°-145° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04102881 |
| Source dataset | uspto-grants-1978_07 |
| ORD ID | ord-e605eaf53e8a4d72bd3be540b5d972d5 |
| Source note | uspto-grants-1978_07 |