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HRID 75682作成日:2026年10月23日

Benzoyl chloride → tert-butyl 5-benzoylhexahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate

https://huagongshe.com/ja/reaction/75682

反応式

関与物質

役割名称HCID仕込み量
反応物Benzoyl chlorideHCID 7412—
反応物TriethylamineHCID 8471—
反応物Tert-butyl octahydropyrrolo(3,4-c)pyrrole-2-carboxylateHCID 4142526—
溶媒TetrahydrofuranHCID 8028—
生成物tert-butyl 5-benzoylhexahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylateHCID 71285668—

反応条件

温度115 °C

反応手順

Et3N (0.5 mL) was added into a solution of tert-butyl hexahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate (0.2 g) and benzoyl chloride (0.11 mL) in THF (10 mL). The mixture was heated to 115° C. for 24 hours. The reaction was quenched with water (10 mL). The aqueous layer was extracted with EtOAc (3×10 mL). The combined organic phase was dried over MgSO4 and concentrated to give a residue which was purified by silica gel chromatography to give tert-butyl 5-benzoylhexahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08835454B2
出典データセットuspto-grants-2014_09
ORD IDord-a75317df12bb404a9f2fa6ebd2c23f0b
出典メモuspto-grants-2014_09