HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → HCID 20323116, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Potassium Nitrate | HCID 24434 | — |
| Reactant | HCID 12923439 | HCID 12923439 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | HCID 20323116 | HCID 20323116 | — |
Reaction Steps
A solution of 3.7 g of 1-methyl-2-chloromethyl-5-phenyl-2,3-dihydro-1H-1,4-benzodiazepine in 20 ml glacial acetic acid and 6 ml concentrated sulfuric acid were reacted at 5° C with a solution of 3.2 g potassium nitrate in 7 ml concentrated sulfuric acid. The reaction mixture was stirred for 1 hour at room temperature, then poured onto ice, made alkaline with dilute sodium hydroxide and extracted with chloroform. The several chloroform extracts were dried and concentrated by evaporation in a vacuum. The residual oil was dissolved in isopropanol and reacted with an ether solution of hydrogen chloride. There were obtained 7-nitro-2-chloromethyl-5-phenyl-2,3-dihydro-1H-1,4-benzodiazepine hydrochloride; m.p. 213° - 214° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04096141 |
| Source dataset | uspto-grants-1978_06 |
| ORD ID | ord-4e89db58b99d42078c775e8aaad15ce9 |
| Source note | uspto-grants-1978_06 |