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HRID 1697718作成日:2026年10月27日

Isopropyl Acetate → 5-(4-tert-Butylphenyl)-4-(phenylsulfonyl)pyrrolidine-2-carboxylic Acid Ethyl Ester

https://huagongshe.com/reaction/1697718

反応式

関与物質

役割名称HCID仕込み量
反応物Isopropyl AcetateHCID 7915—
反応物TriethylamineHCID 8471—
反応物Phenyl vinyl sulfoneHCID 79664—
反応物Lithium BromideHCID 82050—
反応物HCID 178472689HCID 178472689—
溶媒TetrahydrofuranHCID 8028—
生成物5-(4-tert-Butylphenyl)-4-(phenylsulfonyl)pyrrolidine-2-carboxylic Acid Ethyl EsterHCID 667708288%

反応手順

To a stirred solution of (E)-ethyl 2-(4-tert-butylbenzylideneamino)acetate (226 mg, 914 umol; example 441a) in THF (5 ml) under an argon atmosphere were added lithium bromide (119 mg, 1.37 mmol), triethylamine (191 ul, 1.37 mmol) and phenyl vinyl sulfone (154 mg, 914 umol; CAS Reg. No. 5535-48-8). The mixture was stirred at ambient temperature for 20 h. iPrOAc (50 ml) and ice water (40 ml) were added and the layers were separated. The organic layer was washed with brine (40 ml), dried over sodium sulfate and filtered. The solvent was removed under reduced pressure to give a yellow oil which was purified by column chromatography (silica gel, iPrOAc/n-heptane) to obtain the title compound (56 mg, 73 umol; 8%) as colorless solid. MS (ESI): m/z=416.2 [M+H]

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08163793B2
出典データセットuspto-grants-2012_04
ORD IDord-4a5887a39fce47c6962960c891c32db4
出典メモuspto-grants-2012_04