HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Phenoxybenzaldehyde → HCID 53817986, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Phenoxybenzaldehyde | HCID 66139 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 2-Butanamine, (S)- | HCID 6713753 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 53817986 | HCID 53817986 | 77% |
Reaction Steps
4-Phenoxybenzaldehyde (8.13 g, 41 mmol) and (S)-sec-butylamine (3 g, 41 mmol) were dissolved in methanol (137 mL) under a nitrogen at room temperature. Sodium cyanoborohydride (2.58 g) was added, and stirring was continued for 18 hours. The solvent was removed, and the residue was suspended in ether, washed with brine and dried over Na2SO4. The ether was evaporated, and the crude product was chromatographed on silica gel eluting with 3% methanol in methylene chloride to provide 7.24 g (77%) of the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05783593 |
| Source dataset | uspto-grants-1998_07 |
| ORD ID | ord-4c7dad8b56bb419d98701823fa76796b |
| Source note | uspto-grants-1998_07 |