HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methoxynaphthalene → 3-Methoxyacenaphthoquinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methoxynaphthalene | HCID 7119 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | Dry ice ethyleneglycol | HCID 86601574 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Methoxyacenaphthoquinone | HCID 2250264 | 67.1% |
Reaction Steps
A solution of 2-methoxynaphthalene (5 g, 31.6 mmol) and oxalyl chloride (11 mL, 126 mmol) in 150 mL of dichloromethane was cooled to −15° C. (CO2/ethylene glycol) under nitrogen. Aluminum trichloride (10.5 g, 79 mmol) was added slowly over 30 minutes. After 3 hours, the mixture was poured onto 100 g of ice. The layers were separated, and the aqueous layer was washed with dichloromethane. The combined organic layers were washed with saturated sodium bicarbonate, water, brine and dried over magnesium sulfate. The solution was concentrated to afford 4.5 g of a solid. The solid was triturated with dichloromethane to give 1.24 g of the title compound as a solid, mp 218-220° C.;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06362181B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-05d9e3fec74d43c59653182e8ac3c7af |
| Source note | uspto-grants-2002_03 |