関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Octane | HCID 356 | — |
| 反応物 | 1,1-Ethanediol, 1,1-diacetate | HCID 222536 | — |
| 反応物 | Magnesium | HCID 5462224 | — |
| 反応物 | HCID 178506009 | HCID 178506009 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | HCID 19705275 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05536725 |
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| 出典データセット | uspto-grants-1996_07 |
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| ORD ID | ord-9cbc6a7e9a65490a9d54e5e56d0bbb5e |
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| 出典メモ | uspto-grants-1996_07 |
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