HuagongsheHuagongshe Chemistry Print Report · For research reference only
Camphor, (-)- → HCID 57292197, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Camphor, (-)- | HCID 444294 | — |
| Reactant | HCID 178418298 | HCID 178418298 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57292197 | HCID 57292197 | — |
Reaction Steps
The resulting THF solution of 1-naphthylmagnesium bromide was cooled to room temperature. Then, a THF (200 ml) solution of (-)-camphor (50 g, 0.328 mol) was added thereto, and the whole was heated under reflux for 72 hours. The reaction was terminated by cooling with ice-water and adding saturated ammonium chloride aq solution. Then, the organic layer was filtered off, and the solid residue was treated with 10% hydrochloric acid and extracted with diethyl ether. The combined organic layer was dried over anhydrous magnesium sulfate and, after filtration, concentrated to give 121 g of a crude (1S)-2-(1-naphthyl)-1,7,7-trimethylbicyclo [2.2.1]-heptan-2-ol as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05369109 |
| Source dataset | uspto-grants-1994_11 |
| ORD ID | ord-3fbdc026031b4eec927943561ea0a7d6 |
| Source note | uspto-grants-1994_11 |