HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → 5,8-Dimethyl-2-naphthaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone | HCID 6775 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Product | 5,8-Dimethyl-2-naphthaldehyde | HCID 14487609 | — |
Reaction Steps
In a nitrogen atmosphere, the obtained aldehyde (20.9 g) was dissolved in dioxane (300 ml). After adding dichlorodicyanobenzoquinone (50.9 g), the resultant mixture was heated under ref lux for 1.5 hr. Then, it was cooled to room temperature by allowing to stand followed by the addition of toluene (500 ml). The resulting precipitate was collected by filtration and washed with toluene several times. The filtrate was concentrated and the resulting crude product was purified by silica gel column chromatography to give 5,8-dimethyl-2-naphtaldehyde (10.3 g) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06258811B1 |
| Source dataset | uspto-grants-2001_07 |
| ORD ID | ord-6294218e16c246ea8157c401ff11b926 |
| Source note | uspto-grants-2001_07 |