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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129467Generated: October 25, 2026

Chlorodifluoromethane → 1-[1-(Difluoromethoxy)naphthalen-2-yl]ethan-1-one

https://huagongshe.com/reaction/129467

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorodifluoromethaneHCID 6372—
ReactantSodium HydroxideHCID 14798—
Reactant1'-Hydroxy-2'-acetonaphthoneHCID 69733—
Solvent1,4-DioxaneHCID 31275—
Product1-[1-(Difluoromethoxy)naphthalen-2-yl]ethan-1-oneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05468751
Source datasetuspto-grants-1995_11
ORD IDord-2b18abdb79884dd28e51164fd3827cd8
Source noteuspto-grants-1995_11