HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → HCID 69670903, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 86665747 | HCID 86665747 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 69670903 | HCID 69670903 | 76.8% |
Reaction Steps
To a suspension of 1-benzenesulfonyl-5-formyl-2-phenylindole (224 mg) in ethanol (2.5 mL) was added sodium borohydride (11.7 mg), and the mixture was stirred at room temperature for one hour. A saturated aqueous ammonium chloride solution was added to the reaction mixture and the resulting mixture was extracted with ethyl acetate. The organic layer was washed with saturated saline, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluting solvent: ethyl acetate-hexane) to obtain the title compound (173 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08680120B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-4a189ab9ee264ab8ad3369313a107619 |
| Source note | uspto-grants-2014_03 |