関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| 反応物 | 8-(2,4,5-Trifluorophenyl)-1,4-dioxaspiro[4.5]decan-8-ol | HCID 57424359 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 8-(2,4,5-Trifluorophenyl)-1,4-dioxaspiro[4.5]dec-7-ene | HCID 57424360 | — |
反応手順
To a round-bottomed flask (3 L) under nitrogen atmosphere equipped with a Dean-Stark trap, toluene (350 mL), para-toluenesulphonic acid monohydrate (p-TSA) (1 g) and 8-(2,4,5-trifluorophenyl)-1,4-dioxaspiro[4.5]decan-8-ol (94.2 g) were added and the mixture was refluxed overnight. Additional p-TSA (1 g) was added. Refluxing was continued overnight and then the reaction was stirred at room temperature for two more days. The reaction mixture was treated with 0.1 N aqueous sodium hydroxide solution (500 mL) and extracted with heptanes (500 m-L). The organic layer was washed with water (3×500 mL), dried over anhydrous sodium sulfate, filtered and evaporated to yield crude product which was purified by column chromatography (silica gel, gradient 2% to 40% ethyl acetate in heptanes) to yield the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07482336B2 |
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| 出典データセット | uspto-grants-2009_01 |
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| ORD ID | ord-0ce8d6623e3b42ecb71a21c146ccdded |
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| 出典メモ | uspto-grants-2009_01 |
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