関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methoxymethyl-triphenylphosphonium chloride | HCID 2723798 | — |
| 反応物 | Potassium tert-butoxide | HCID 23665647 | — |
| 反応物 | HCID 178509796 | HCID 178509796 | — |
| 反応物 | HCID 178509797 | HCID 178509797 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | HCID 178494963 | HCID 178494963 | 82% |
反応手順
Commercially available methoxymethyltriphenylphosphonium chloride (257 g, 0.75 mol) was added to tetrahydrofuran (500 ml), followed by adding potassium t-butoxide (84.2 g, 0.75 mol) in argon atmosphere with stirring at -10° C. over 40 minutes, agitating the reaction solution at 0° C. for one hour, dropwise adding a solution of 3-[trans-4-(4-cyanophenyl)cyclohexyl]-1-propanal (121 g, 0.50 mol) obtained according to the method of Example 3 (i), in tetrahydrofuran (400 ml) at -10° C. over one hour, agitating the reaction mixture at 0° C. for one hour, further agitating at 20° C. for 2 hours, adding toluene (1 l) and water (1 l) to the reaction mixture at 0° C., four times washing the resulting toluene solution with water (1 l), drying over anhydrous magnesium sulfate, separating the drying agent, distilling off toluene, purifying the resulting residue according to silica gel column chromatography using heptane as an eluent to obtain trans-1-(4-methoxy-3-butenyl)-4-(4-cyanophenyl)cyclohexane (110.8 g, 0.41 mol), adding to the total quantity of this compound, tetrahydrofuran (1.5 l) and 2N-hydrochloric acid (0.4 l), heating the mixture under reflux, with stirring for one hour, cooling the resulting reaction mixture, adding diethyl ether (0.5 l) and water (1 l), three times washing the resulting diethyl ether solution with water (0.5 l), drying over anhydrous magnesium sulfate, separating the drying agent, concentrating under reduced pressure to obtain a residue (120 g), and recrystallizing from a mixed solvent of heptane and ethyl acetate (3:1) to obtain 4-[trans-4-(4-cyanophenyl)cyclohexyl]-1-butanal (93.0 g, 0.36 mol).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05053162 |
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| 出典データセット | uspto-grants-1991_10 |
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| ORD ID | ord-58a57e4b41434b3aaa03d02738fa1272 |
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| 出典メモ | uspto-grants-1991_10 |
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