HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → (4-Methoxyphenyl)(2-phenylnaphthalen-1-yl)methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone | HCID 6775 | — |
| Reactant | (4-Methoxyphenyl)(2-phenyl-3,4-dihydronaphthalen-1-yl)methanone | HCID 12835030 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | (4-Methoxyphenyl)(2-phenylnaphthalen-1-yl)methanone | HCID 22001239 | — |
Reaction Steps
To 30 ml. of dioxane were added 1.90 grams (5.58 mmoles) of 3-phenyl-4-(4-methoxybenzoyl)-1,2-dihydronaphthalene (prepared as in Example 3) and 2.00 grams (8.81 mmoles) of 2,3-dichloro-5,6-dicyano-1,4-benzoquinone. The resulting mixture was heated at reflux for twelve hours in a nitrogen atmosphere. The mixture then was cooled and evaporated to dryness. Water and ether were added to the residue. The ether layer was separated and washed 5 times with 20 ml. portions of 5 N sodium hydroxide and then with aqueous sodium chloride. The mixture then was dried over magnesium sulfate and evaporated to give 1.9 grams of substantially pure 1-(4-methoxybenzoyl)-2-phenylnaphthalene as a green oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04400543 |
| Source dataset | uspto-grants-1983_08 |
| ORD ID | ord-78c756fed1a74c0d81bdd30c7be81beb |
| Source note | uspto-grants-1983_08 |