関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Tetrafluoroboric acid | HCID 28118 | — |
| 反応物 | 2-Cyclopentene-1-acetic acid | HCID 96216 | — |
| 反応物 | Iodo benzene diacetate | HCID 12217721 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 生成物 | Ctk1B5122 | HCID 11126247 | — |
反応手順
Tetrafluoroboric acid (2.50 mL, 15.9 mmol) was added to a solution of iodobenzene diacetate (5.10 g, 15.9 mmol) in acetic acid (13.2 mL). 2-Cyclopentene-1-acetic acid (955 μL, 7.93 mmol) was added and the solution was stirred at room temperature for 1 hour. The solution was then added to water and extracted with chloroform. The chloroform layer was extracted with water. The combined organic layers were dried (magnesium sulfate), filtered, and concentrated in vacuo. The residue was purified by silica gel chromatography (Biotage 40M), eluting with 0-100% ethyl acetate/hexanes to give the title compound as a colorless oil. 1H NMR (500 MHz, CHCl3) δ 2.22-2.31 (m, 2H), 2.67-2.84 (m, 2H), 3.05-3.15 (m, 1H), 5.44-5.51 (m, 1H), 5.79-5.86 (m, 1H), 6.01-6.07 (m, 1H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08530521B2 |
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| 出典データセット | uspto-grants-2013_09 |
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| ORD ID | ord-7aaa0f4440d44075bea17a6b45e2a5f2 |
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| 出典メモ | uspto-grants-2013_09 |
|---|