HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → (2-Methyl-1-naphthyl)(phenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | 1-Bromo-2-methylnaphthalene | HCID 75754 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-Methyl-1-naphthyl)(phenyl)methanol | HCID 19957120 | 78.7% |
Reaction Steps
A solution of 10 g (45 mmol) of 1-bromo-2-methylnaphthalene in 75 mL of THF was refluxed with 1.2 g (50 mmol) of magnesium turnings for three hours. The reaction was cooled on ice and 4.8 mL (43 mmol) of benzaldehyde was added. The ice was removed, the reaction was stirred 45 minutes and quenched with 5 mL of 1N HCl followed by 50 mL of water. The reaction was extracted into ethyl acetate, dried over sodium sulfate and flash chromatographed through silica gel with 5-10% ethyl acetate in hexane to provide 8.4 g (75%) of 2-methyl-a-phenyl-1-naphthalenemethanol as a pale yellow gum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05624922 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-0c4660183fbc41969b1652484277c365 |
| Source note | uspto-grants-1997_04 |