HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 13714726, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-(2-Nitrophenoxy)propylamine | HCID 5276874 | — |
| Reactant | HCID 14000643 | HCID 14000643 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 13714726 | HCID 13714726 | 52.8% |
Reaction Steps
A solution of 8.09 g of 4-cyano-4-isopropyl-4-(3,4,5-trimethoxyphenyl)butyraldehyde and 4.96 g of 3-(2-nitrophenoxy)-propylamine in 100 ml of methanol was refluxed for 3 hours. After cooling, to the solution was added 0.50 g of sodium borohydride and the solution was stirred overnight at room temperature. The solvent was removed and to the residue was added water. The solution was extracted with chloroform and the extract was washed with water, dried, and evaporated. The residue was chromatographed on silica gel using 10% methanol-chloroform as an eluent to give 6.48 g of the desired compound as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04612329 |
| Source dataset | uspto-grants-1986_09 |
| ORD ID | ord-285edd3b3abc4dd997fce3177e670764 |
| Source note | uspto-grants-1986_09 |