HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Lutidine → 3-(Tetrahydro-2-furanyl)phenylmethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | 3-(Dihydro-2-furanyl)benzaldehyde | HCID 21981090 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(Tetrahydro-2-furanyl)phenylmethanol | HCID 23506104 | 70% |
Reaction Steps
Ex-608C) A THF (15 mL) solution of the aldehyde from EX-608B (0.70 g, 4.0 mmol) and 2,6-lutidine (0.46 mL, 4.0 mmol) was stirred in a hydrogen atmosphere (50 psi) in the presence of 10% Pd/C (0.29 g) for 18 h at room temperature. The slurry was filtered through celite, and the solvent was removed. The residue was taken up in ethyl acetate and washed with 1 N HCl and brine. The organic layer was dried (MgSO4) and evaporated to give 0.50 g (70%) of the desired 3-(tetrahydro-2-furanyl)phenylmethanol product as a yellow oil. The formation of the desired product was monitored by the disappearance of the aldehyde (δ˜10) and olefin peaks in the 1H NMR spectrum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06699898B2 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-797a3c12cee44018b8bd94149b3d26bd |
| Source note | uspto-grants-2004_03 |