HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → HCID 70296592, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 54459417 | HCID 54459417 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 70296592 | HCID 70296592 | 70.5% |
Reaction Steps
To a solution of 5.35 g (14.3 mmoles) of 1-[2-(1-naphtyl)-vinyl]-4-methyl-7,8-dimethoxy-5H-2,3-benzodiazepine in 30 ml of glacial acetic acid a solution of 1.76 g (46.3 mmoles) of sodium borohydride in 10 ml of water is dropped at 50° C., under stirring, and the reaction mixture is stirred further for 2 hours. The product is then stirred with 250 ml of water, made alkaline with ammonium hydroxide solution, the separated yellow precipitate is filtered, washed with water and recrystallized from isopropanol. Thus 3.75 g (70.5%) of the desired compound are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06075018 |
| Source dataset | uspto-grants-2000_06 |
| ORD ID | ord-7109163f3e6a4e6d958dd142341144dc |
| Source note | uspto-grants-2000_06 |