HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 13228378, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 13228374 | HCID 13228374 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 13228378 | HCID 13228378 | — |
Reaction Steps
Portionwise 0.2 g (52 mmol) of sodium borohydride was added to a solution of 3.0 g (6.3 mmol) of 8-chloro-6-(2-chlorophenyl)-2,5-dimethyl-2H,4H-pyrrolo[3,4-d][2]benzazepin-5-ium iodide in 50 ml of methanol which was cooled to 0°. The mixture was stirred at 0° for 20 min followed by the removal of the methanol at reduced pressure. The residue was partitioned between methylene chloride and water. The methylene chloride solution was washed with water and saturated aqueous sodium chloride, dried over anhydrous sodium sulfate, and concentrated at reduced pressure to give a pale yellow oil. Crystallization from ether gave colorless crystals, mp 154°-155°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04409390 |
| Source dataset | uspto-grants-1983_10 |
| ORD ID | ord-f02549c6eb8c4949857e89c3ac08d9ac |
| Source note | uspto-grants-1983_10 |