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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 727172생성일: 2026년 10월 26일

Hydrochloric Acid → HCID 19705275, 화합물

https://huagongshe.com/reaction/727172

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물OctaneHCID 356—
반응물1,1-Ethanediol, 1,1-diacetateHCID 222536—
반응물MagnesiumHCID 5462224—
반응물HCID 178506009HCID 178506009—
용매TolueneHCID 1140—
생성물HCID 19705275HCID 19705275—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05712281
출처 데이터셋uspto-grants-1998_01
ORD IDord-eb8dc086490948328eef38c2e3e2bf3b
출처 메모uspto-grants-1998_01