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HRID 253548作成日:2026年10月26日

Ammonium Chloride → Tert-butyl 3-benzoylpyrrolidine-1-carboxylate

https://huagongshe.com/reaction/253548

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物Tert-butyl 3-[methoxy(methyl)carbamoyl]pyrrolidine-1-carboxylateHCID 57419605—
反応物HCID 178418255HCID 178418255—
溶媒TetrahydrofuranHCID 8028—
生成物Tert-butyl 3-benzoylpyrrolidine-1-carboxylateHCID 5741960684%

反応手順

A stirred solution of tert-butyl 3-(methoxy(methyl)carbamoyl)pyrrolidine-1-carboxylate (2.27 g, 8.8 mmol) in dry THF (40 mL) was cooled in an ice bath and 1 M PhMgBr in THF (20 mL, 20.0 mmol) was added dropwise over 2 min. The mixture was stirred and the ice bath was allowed to melt. After 3 h, the mixture was poured into satd aq NH4Cl and extracted with ether (2×200 mL). The combined ether extracts were dried over MgSO4 and concentrated to leave an oil. Flash chromatography on a 40-g silica cartridge eluted with a 0 to 50% EtOAc in hexanes gradient afforded tert-butyl 3-benzoylpyrrolidine-1-carboxylate (2.04 g, 84%) as a clear colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07872028B2
出典データセットuspto-grants-2011_01
ORD IDord-5d615d594bd84870829e90a9238e3944
出典メモuspto-grants-2011_01