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HRID 1735306作成日:2026年10月25日

Hydrochloric Acid → HCID 19705275、化合物

https://huagongshe.com/reaction/1735306

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物OctaneHCID 356—
反応物1,1-Ethanediol, 1,1-diacetateHCID 222536—
反応物MagnesiumHCID 5462224—
反応物HCID 178506009HCID 178506009—
溶媒TolueneHCID 1140—
生成物HCID 19705275HCID 19705275—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05536725
出典データセットuspto-grants-1996_07
ORD IDord-9cbc6a7e9a65490a9d54e5e56d0bbb5e
出典メモuspto-grants-1996_07