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HRID 18926作成日:2026年10月26日

Benzyl chloroformate → methyl 3-(benzyloxycarbonyl)-5-tert-butyl-1H-pyrrole-2-carboxylate

https://huagongshe.com/reaction/18926

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl chloroformateHCID 10387—
反応物Sodium hydrideHCID 24758—
反応物methyl 3-amino-5-(tert-butyl)-1H-pyrrole-2-carboxylateHCID 18322367—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物methyl 3-(benzyloxycarbonyl)-5-tert-butyl-1H-pyrrole-2-carboxylateHCID 68682038—

反応手順

A mixture of the previously prepared methyl 3-amino-5-tert-butyl-1H-pyrrole-2-carboxylate (0.400 g, 2.0 mmol) and NaH (60% w/w, 0.760 g, 4.5 mmol) in THF (4 mL) was stirred at room temperature for 30 min. To the resulting mixture was added benzyl carbonochloridate drop wise and stirred at room temperature overnight. The reaction mixture was diluted with ethyl acetate and washed with saturated sodium bicarbonate solution. The crude product was recrystallized from dichloromethane:hexane to afford the desired methyl 3-(benzyloxycarbonyl)-5-tert-butyl-1H-pyrrole-2-carboxylate (0.560 g) as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741479B2
出典データセットuspto-grants-2010_06
ORD IDord-15201a1c4ea34fa8bc1c4db79bf5c082
出典メモuspto-grants-2010_06