関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Carbon Dioxide | HCID 280 | — |
| 反応物 | Water | HCID 962 | — |
| 反応物 | 4-Bromo-2-fluoro-1-(pentafluoroethyl)benzene | HCID 86661427 | — |
| 反応物 | HCID 178418918 | HCID 178418918 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 3-Fluoro-4-(pentafluoroethyl)benzoic acid | HCID 86661428 | — |
反応手順
A solution of 16.0 g (99% by weight; 54.1 mmol) of 3-fluoro-4-(pentafluoroethyl)-bromobenzene in 110 ml of tetrahydrofuran was cooled to −10° C. Added dropwise over the course of 30 minutes were 36.8 ml of a 2M (73.6 mmol) solution of isopropylmagnesium chloride. The mixture was stirred at −10° C. for 2.5 hours and then cautiously poured onto an excess of dry ice. Then, 130 ml of water were added, and the mixture was subsequently extracted once with 10 ml of diethyl ether. The aqueous phase was acidified with half-concentrated hydrochloric acid and then extracted with four times 150 ml of diethyl ether. The combined organic phases were dried and the filtrate was freed from the solvent. The residue was recrystallized from chloroform, giving 10.7 g of product with a purity of 98% by weight.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08603947B2 |
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| 出典データセット | uspto-grants-2013_12 |
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| ORD ID | ord-91da815e66bd4776a8207ac8993ab984 |
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| 出典メモ | uspto-grants-2013_12 |
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