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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727172Generated: October 26, 2026

Hydrochloric Acid → HCID 19705275, compound

https://huagongshe.com/reaction/727172

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantOctaneHCID 356—
Reactant1,1-Ethanediol, 1,1-diacetateHCID 222536—
ReactantMagnesiumHCID 5462224—
ReactantHCID 178506009HCID 178506009—
SolventTolueneHCID 1140—
ProductHCID 19705275HCID 19705275—

Reaction Steps

Under a nitrogen atmosphere, the reaction mixture from above is decanted into a clean, dry reaction vessel, leaving the unreacted magnesium turnings in the first vessel. This solution containing 2,2,3,3-tetrafluoro-2,3-dihydrobenzofuran-7-ylmagnesium chloride is heated at reflux, and 16.5 grams (0.55 mole based on formaldehyde) of polyoxymethylene diacetate (avg. mol. wgt. approx. 50,000, commercially available from E. I. du Pont De Nemours & Co., Inc. Wilmington Del., under the trade name Delrin 500 acetal homopolymer resin), milled to about 80 mesh, is added with stirring during about a three hour period. Upon completion of addition, the reaction mixture is heated at reflux for an additional four hours and then is allowed to cool to ambient temperature as it stood for about 18 hours. The reaction mixture is warmed to about 53° C. and then is poured into 100 grams of ice, 52 grams of concentrated hydrochloric acid, and 200 grams of a mixture of 95% n-octane and 5% toluene (wt/wt). This mixture is filtered, and the organic layer is separated. The organic layer is concentrated under reduced pressure, yielding 2,2,3,3-tetrafluoro-2,3-dihydrobenzofuran-7-ylmethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05712281
Source datasetuspto-grants-1998_01
ORD IDord-eb8dc086490948328eef38c2e3e2bf3b
Source noteuspto-grants-1998_01