HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2,3-Dibutoxy-6-chloronaphthalene-1,4-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2,3,6-Trichloronaphthalene-1,4-dione | HCID 12660249 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2,3-Dibutoxy-6-chloronaphthalene-1,4-dione | HCID 13660376 | 68.2% |
Reaction Steps
To a solution of sodium-n-butoxide (25.8 g) in dry dimethylformamide (125 ml) was added 2,3,6-trichloro-1,4-naphthoquinone (28 g) in one amount. The mixture was refluxed for 2 hours, then cooled, acidified with 6M hydrochloric acid and evaporated. The residue was chromatographed over silica gel using dichloromethane as eluant to yield 2,3-di-n-butoxy-6-chloro-1,4-naphthoquinone (12.3 g) as a red oily solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04946845 |
| Source dataset | uspto-grants-1990_08 |
| ORD ID | ord-ff5029b4256c446c82950ac7d8d75403 |
| Source note | uspto-grants-1990_08 |