関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Diethyl (cyanomethyl)phosphonate | HCID 75676 | — |
| 反応物 | 1,1-Bis(propan-2-yl) 3-oxocyclobutane-1,1-dicarboxylate | HCID 4913357 | — |
| 反応物 | Potassium tert-butoxide | HCID 23665647 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | Diisopropyl 3-(cyanomethylene)cyclobutane-1,1-dicarboxylate | HCID 66823993 | 90.8% |
反応手順
To a mixture of 1.0000 M of potassium tert-butoxide in tetrahydrofuran (17 mL) and THF (10 mL) was added dropwise, at 0° C., diethyl cyanomethylphosphonate (2.7 mL, 0.017 mol). The reaction was warmed to rt and 30 min later cooled to 0° C. again. To the reaction mixture was added a solution of diisopropyl 3-oxocyclobutane-1,1-dicarboxylate (2.7 g, 0.011 mol) in THF (10 mL). The reaction was allowed to warm up to rt gradually and stirred at rt for 2 h. The reaction was quenched with saturated aq. NH4Cl and the organic solvent was reduced. The mixture was extracted with EtOAc. The combined organic layers were washed with brine, dried over MgSO4, concentrated and purified with Combiflash (silica gel, 0-35% EtOAc/Hex) to give the desired product (2.65 g) as light yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08420629B2 |
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| 出典データセット | uspto-grants-2013_04 |
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| ORD ID | ord-bdfe24814a8b481bbee138337cd49553 |
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| 出典メモ | uspto-grants-2013_04 |
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