HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(2-quinolinylmethoxy)Benzaldehyde → 4-Phenyl-1-(4-(2-quinolinylmethoxy)phenyl)butanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(2-quinolinylmethoxy)Benzaldehyde | HCID 14578960 | — |
| Reactant | HCID 178418471 | HCID 178418471 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Phenyl-1-(4-(2-quinolinylmethoxy)phenyl)butanol | HCID 10068544 | — |
Reaction Steps
To a solution of the aldehyde from Step I, (1.34 g) in THF at 0° was added dropwise the 3-phenylpropylmagnesium bromide (1.1 mol. equiv., from above). After 30 mins, the reaction was quenched by the addition of 25% aqueous NH4OAc solution. The mixture was then extracted with ethyl acetate (×2), the organic phase was washed with brine (×2), dried and evaporated under reduced pressure. The title compound was obtained after recrystallization from ethyl acetate/hexane, m.p. 118°-119°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05102881 |
| Source dataset | uspto-grants-1992_04 |
| ORD ID | ord-f8e9c0338efd461ca9656e4de428a8dd |
| Source note | uspto-grants-1992_04 |