HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexanone → HCID 15617826, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexanone | HCID 7967 | — |
| Reactant | 1-(methoxymethoxy)naphthalene | HCID 10779684 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 15617826 | HCID 15617826 | 58% |
Reaction Steps
A solution of 1-methoxymethoxy-naphthalene (3.76 g, 0.020 mole) in dry ether (40 mL) was treated with n-butyllithium (1.6M in hexane: 25.0 mL, 0.040 mole) at room temperature over a period of 15 minutes. After stirring for an additional 1.5 hours, a solution of cyclohexanone (4.90 g, 0.050 mole) in either (15 mL) was added and the resulting mixture was stirred at room temperature for 2 hours. It was then quenched with saturated aqueous ammonium chloride and the crude product was isolated by extraction with ether. Chromatography with 9:1 hexane/ethyl acetate provided the title compound as a colorless oil (3.30 g, 58%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04985442 |
| Source dataset | uspto-grants-1991_01 |
| ORD ID | ord-351b5d1b11794fe988bd3c65f1b77d17 |
| Source note | uspto-grants-1991_01 |