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HRID 2213663作成日:2026年10月25日

tert-Butyl 2-formyl-1H-pyrrole-1-carboxylate → [N-(dimethylethoxycarbonyl)pyrrol-2-yl](3-aminophenyl)methanol

https://huagongshe.com/reaction/2213663

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butyl 2-formyl-1H-pyrrole-1-carboxylateHCID 5057005—
反応物HCID 178504299HCID 178504299—
溶媒TetrahydrofuranHCID 8028—
生成物[N-(dimethylethoxycarbonyl)pyrrol-2-yl](3-aminophenyl)methanolHCID 21957618—

反応条件

温度0 °C

反応手順

A solution of N-(dimethylethoxycarbonyl)pyrrole-2-carboxaldehyde (10 g, 50 mmol) in THF (500 mL) at −30° C. under nitrogen was added dropwise to 3-[bis(trimethylsilyl)amino]phenylmagnesium chloride (55 mL of a 1M solution in THF, 55 mmol). After addition the reaction mixture was gradually warmed up and stirred at 0° C. for 1 hour, then at ambient temperature for 15 minutes. The reaction mixture was poured into ice water, and stirred for 30 minutes. The reaction mixture was extracted with ethyl ether (1 L). The combined organic layers were dried (Na2SO4) and concentrated. Chromatography on SiO2 (700 g) using 1:1 hexane/ethyl acetate afforded [N-(dimethylethoxycarbonyl)pyrrol-2-yl](3-aminophenyl)methanol (11.2 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07105563B2
出典データセットuspto-grants-2006_09
ORD IDord-4522992528e14ea8babc3e79fad1260f
出典メモuspto-grants-2006_09