関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Triethyl phosphonoacetate | HCID 13345 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | Lithium diisopropylamide | HCID 2724682 | — |
| 反応物 | 2-(3-Methoxyphenyl)-2-methylpropanal | HCID 13296993 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Tetrahydrofuran heptane ethylbenzol | HCID 22742125 | — |
| 生成物 | ethyl-E-4-(3-methoxyphenyl)-4-methylpent-2-enoate | HCID 86599931 | 95.8% |
反応手順
33.6 g (114.3 mmol) of phosphonoacetic acid triethyl ester is introduced into 148 ml of tetrahydrofuran. At 0° C., 79.7 ml of a 2 M solution of LDA in THF/heptane/ethylbenzene is added in drops (1½ hours). After one hour of stirring, 24.3 g (136.34 mmol) of 2-(3-methoxyphenyl)-2-methylpropanal, dissolved in 130 ml of tetrahydrofuran, is added in drops at 0° C. After five days of stirring at room temperature, the reaction mixture is poured into 250 ml of dilute ammonium chloride solution and extracted twice with 400 ml each of diethyl ether. The combined organic extracts are treated as usual, and the residue that is obtained is chromatographed on silica gel (mobile solvent ethyl acetate/hexane). 27.2 g (80.4%) of the desired compound is isolated.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07638515B2 |
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| 出典データセット | uspto-grants-2009_12 |
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| ORD ID | ord-a6c56cfdff1a452ab8f8c13c4eed5ba2 |
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| 出典メモ | uspto-grants-2009_12 |
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