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HRID 53904作成日:2026年10月27日

Sodium Sulfite → 4-(2-Benzoylpyrrol-1-yl)-2-iodobutyric acid methyl ester

https://huagongshe.com/reaction/53904

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium SulfiteHCID 24437—
反応物Iodine chlorideHCID 24640—
反応物SodiumHCID 5360545—
反応物2-Benzoyl-1-[2-(2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-yl)ethyl]pyrroleHCID 10914795—
溶媒MethanolHCID 887—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
生成物Sodium MethoxideHCID 10942334—
生成物4-(2-Benzoylpyrrol-1-yl)-2-iodobutyric acid methyl esterHCID 5406994191.5%

反応条件

温度-30 °C

反応手順

Sodium methoxide solution was prepared by dissolving metallic sodium (1.38 g, 60 mmol) in methanol (30 mL). This solution was diluted with anhydrous tetrahydrofuran (100 mL) and cooled to -30° C. A solution of iodine monochloride (8.97 g, 55.3 mmol) in dichloromethane (30 mL) was added dropwise to the stirred alkoxide solution. The resulting solution was stirred for 2 minutes, then the sodium salt of 1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-benzoylpyrrole (VI, 18.15 g, 50 mmol) was added as a solid. The mixture was stirred for 90 minutes at -30° C., then allowed to warm to 22° C. and stirred for an additional 18 hours. The reaction mixture was poured into 150 mL of 2% aqueous sodium sulfite solution in a separatory funnel, and the reaction flask was washed with 10 mL of diethyl ether, which was added to the separatory funnel. The mixture was shaken thoroughly, and the phases were separated. The aqueous phase was extracted with diethyl ether (2×20 mL), and the combined organic phase was washed with brine, dried over magnesium sulfate, and evaporated to afford 4-(2-benzoylpyrrol-1-yl)-2-iodobutyric acid methyl ester (IV, 18.16 g, 91.5%), identical to the material prepared by the method described above.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05621115
出典データセットuspto-grants-1997_04
ORD IDord-f14f0b2044454b238289b5666ea71862
出典メモuspto-grants-1997_04