関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | 2,6-Dihydroxybenzoic Acid | HCID 9338 | — |
| 反応物 | 2-Fluoroethyl bromide | HCID 12982 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | 2-Fluoroethyl 2,6-di(2-fluoroethoxy)benzoate | HCID 15058703 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 2,6-Di(2-fluoroethoxy)benzoic acid | HCID 15058702 | 51% |
反応手順
To a stirred solution of 3.0 grams (0.075 mole) of sodium hydroxide in 150 ml of ethanol was added 11.3 grams (0.039 mole) of 2-fluoroethyl 2,6-di(2-fluoroethoxy)benzoate (prepared by the method of Step A of Example 13 from 2,6-dihydroxybenzoic acid and three equivalents of 1-bromo-2-fluoroethane). The reaction mixture was stirred at room temperature for approximately 48 hours. The reaction mixture was filtered, and the filter cake was saved. The filtrate was evaporated under reduced pressure leaving a residue. The filter cake and residue were added to 200 ml of an aqueous, 10% hydrochloric acid solution. The resultant mixture was stirred at room temperature and was extracted with several portions of methylene chloride. The extracts were combined and dried over anhydrous magnesium sulfate. The dried organic phase was filtered, and the filtrate was evaporated under reduced pressure to yield 4.9 grams of 2,6-di(2-fluoroethoxy)benzoic acid as a solid, mp 57°-58° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04960884 |
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| 出典データセット | uspto-grants-1990_10 |
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| ORD ID | ord-94f77d4fec884cf2aa5ba069745f4405 |
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| 出典メモ | uspto-grants-1990_10 |
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