HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorodifluoromethane → 1-[1-(Difluoromethoxy)naphthalen-2-yl]ethan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorodifluoromethane | HCID 6372 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1'-Hydroxy-2'-acetonaphthone | HCID 69733 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1-[1-(Difluoromethoxy)naphthalen-2-yl]ethan-1-one | HCID 2360828 | — |
Reaction Steps
10 g of 1-hydroxy-2-acetylnaphthalene are dissolved in 60 ml of dioxane, and 30 ml of 30% sodium hydroxide solution are added. At a temperature of from 70° C. to 80° C., difluorochloromethane (Freon 22) is introduced until no further absorption is observed. The dioxane phase is then decanted, the NaOH phase is washed with dioxane, the dioxane phase is decanted, and the combined dioxane solutions are largely concentrated in vacuo using a rotary evaporator. Water is added to the residue, the mixture is extracted several times with diethyl ether, and the diethyl ether solution is dried over Na2SO4, filtered and concentrated by evaporation. The residue is recrystallised from diethyl ether/hexane. Yield: 4 g, m.p. 80°-81° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05468751 |
| Source dataset | uspto-grants-1995_11 |
| ORD ID | ord-2b18abdb79884dd28e51164fd3827cd8 |
| Source note | uspto-grants-1995_11 |