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Tetrahydrofuran → 1-(3-Tert-butyl-phenyl)-3-methylene-cyclohexanecarboxylic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| 反応物 | 1-(3-Tert-butyl-phenyl)-3-methylene-cyclohexanecarboxylic acid 2-trimethylsilanyl-ethyl ester | HCID 59733770 | — |
| 生成物 | 1-(3-Tert-butyl-phenyl)-3-methylene-cyclohexanecarboxylic acid | HCID 59733731 | 107.2% |
反応手順
A 1.0 M solution of tetrabutylammonium fluoride in tetrahydrofuran (15.0 mL, 15.0 mmol) was added to 1-(3-tert-butyl-phenyl)-3-methylene-cyclohexanecarboxylic acid 2-trimethylsilanyl-ethyl ester (2.67 mg, 7.16 mmol). After stirring for 16 h, the solution was concentrated, diluted with 10% aqueous hydrochloric acid, and extracted with diethyl ether. The combined organic extracts were dried over magnesium sulfate, filtered, and concentrated to yield 2.09 g (100% yield) of 1-(3-tert-butyl-phenyl)-3-methylene-cyclohexanecarboxylic acid as a yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07385085B2 |
| 出典データセット | uspto-grants-2008_06 |
| ORD ID | ord-89e0d65b0b0a4531a37e2452c69aba3f |
| 出典メモ | uspto-grants-2008_06 |