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HRID 1966159作成日:2026年10月26日

Diethyl (cyanomethyl)phosphonate → Diisopropyl 3-(cyanomethylene)cyclobutane-1,1-dicarboxylate

https://huagongshe.com/reaction/1966159

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl (cyanomethyl)phosphonateHCID 75676—
反応物1,1-Bis(propan-2-yl) 3-oxocyclobutane-1,1-dicarboxylateHCID 4913357—
反応物Potassium tert-butoxideHCID 23665647—
溶媒TetrahydrofuranHCID 8028—
生成物Diisopropyl 3-(cyanomethylene)cyclobutane-1,1-dicarboxylateHCID 6682399390.8%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US08420629B2
出典データセットuspto-grants-2013_04
ORD IDord-bdfe24814a8b481bbee138337cd49553
出典メモuspto-grants-2013_04