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HRID 418891作成日:2026年10月26日
Acetic acid, 2-(triphenylphosphoranylidene)-, ethyl ester → Ethyl [2-(3-methoxyphenyl)-cyclohexylidene]acetate
https://huagongshe.com/reaction/418891
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Acetic acid, 2-(triphenylphosphoranylidene)-, ethyl ester | HCID 70670 | — |
| 反応物 | 2-(3-Methoxyphenyl)cyclohexanone | HCID 85868 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | Ethyl [2-(3-methoxyphenyl)-cyclohexylidene]acetate | HCID 53720108 | 99.8% |
反応手順
Combine 2-(3-methoxyphenyl)-cyclohexanone (5.0 g, 24.5 mmol), carbethoxymethylene triphenylphosphorane (15.4 g, 44.1 mmol), and toluene (150 mL), stir and heat at reflux. After 22 hours, cool to ambient temperature and concentrate under vacuum. Add ether and filter off the triphenylphosphine oxide precipitate and concentrate the ether filtrate. Flash chromatograph with 0% to 10% ethyl acetate/hexanes to yield the titled compound (6.71 g, 99%) as a clear oil. TLC Rf=0.58 in 8:1 hexanes:ethyl acetate. 1H NMR (CDCl3): 7.25 (m, 1H), 6.81-6.79 (m, 3H), 6.73 (s, 1H), 5.14 (s, 1H), 4.07 (q, J=14.4, 7.2, 2H), 3.80 (s, 3H), 3.80-3.69 (m, 1H), 3.39-3.36 (m, 1H), 2.20-2.16 (m, 1H), 2.06-2.03 (m, 1H), 1.96-1.87 (m, 3H), 1.65-1.54 (m, 2H), 1.2 (t, J=1.2, 8, 3H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08093302B2 |
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| 出典データセット | uspto-grants-2012_01 |
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| ORD ID | ord-3a614e1f23b448ef9a48160ce7b521bf |
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| 出典メモ | uspto-grants-2012_01 |
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