HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 22458855, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 22458811 | HCID 22458811 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 22458855 | HCID 22458855 | 66.1% |
Reaction Steps
To a solution of N-(9-Ethyl-6-formyl-9H-carbazol-3-yl)-acetamide (50 mg, 0.150 mmol) in EtOH (5 ml) at 0° C. was added NaBH4 (8.5 mg, 0.225 mmol), and after 10 minutes the cooling bath was removed. After 1 hour additional NaBH4 (2 mg) was added, and after stirring 90 minutes water was added, the EtOH removed in vacuo, and the aqueous layer extracted with CH2Cl2. The organic layer was dried (Na2SO4) and concentrated to afford the crude product. Chromatographic purification (silica, 50% EtOAc/Hex) afforded the product as a solid (28 mg, 56% yield). MS m/z @ 337 (m+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06399631B1 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-dbb9095b484f4e7d88e6888690f29c73 |
| Source note | uspto-grants-2002_06 |