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HRID 465401作成日:2026年10月25日

Water → Methyl 4-methoxyvinylpyrrole-2-carboxylate

https://huagongshe.com/reaction/465401

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物methyl 4-formyl-1H-pyrrole-2-carboxylateHCID 640310—
反応物Methoxymethyl-triphenylphosphonium chlorideHCID 2723798—
反応物Lithium diisopropylamideHCID 2724682—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 4-methoxyvinylpyrrole-2-carboxylateHCID 5705293450%

反応手順

Into a solution of 200 g (0.58 mol) of methoxymethyltriphenylphosphonium chloride in 1.5 liter of tetrahydrofuran, was added dropwise 220 ml of a tetrahydrofuran solution (2.01 mol concentration) containing 0.44 mol of lithium diisopropylamide under stirring and cooling with ice. After one-hour stirring at room temperature, 400 ml of a tetrahydrofuran solution of 57.6 g (0.38 mol) of methyl 4-formylpyrrole-2-carboxylate was added to the mixture at 5° to 8° C. under cooling with ice. The reaction was carried out for one hour at room temperature, and the reaction mixture was added with water and extracted with ethyl acetate. The organic layer was collected, washed with a saturated solution of sodium chloride, dried over anhydrous magnesium sulfate and evaporated to obtain a residue. The residue was purified by a silica-gel column chromatography (eluent:ethyl acetate/hexane=1/4) to obtain 34.4 g of methyl 4-methoxyvinylpyrrole-2-carboxylate as a mixture of E-isomer and Z-isomer. The yield was 50%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05153217
出典データセットuspto-grants-1992_10
ORD IDord-b41ebea4fbc4487888a260c49161bb9c
出典メモuspto-grants-1992_10