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HRID 655161作成日:2026年10月23日

3-Iodopyridine → (1S,4S)-4-(3-pyridyl)-2-cyclopenten-1-ol

https://huagongshe.com/ja/reaction/655161

反応式

関与物質

役割名称HCID仕込み量
反応物3-IodopyridineHCID 70714—
反応物rac-(1R,4S)-4-hydroxycyclopent-2-en-1-yl acetateHCID 10154103—
反応物HCID 178418546HCID 178418546—
反応物HCID 178418918HCID 178418918—
溶媒TetrahydrofuranHCID 8028—
溶媒Ammonium ChlorideHCID 25517—
生成物(1S,4S)-4-(3-pyridyl)-2-cyclopenten-1-olHCID 5948612155.3%

反応手順

To a solution of 3-Iodopyridine (13.0 g, 63.3 mmol) in THF (30 mL) was added i-PrMgCl (38.0 mL, 76.0 mmol) at 3-9° C. After stirring was continued at room temperature for 30 min, CuCN (567 mg, 6.33 mmol) was added to the solution at 2° C. After stirring was continued at 3° C. for 30 min, to the resulting solution were added (1R,4S)-4-hydroxycyclopent-2-enyl acetate (3.00 g, 21.1 mmol) in THF (30 mL). The whole mixture was stirred at the room temperature for 2 h, and diluted with saturated NH4Cl with vigorous stirring. The products were extracted with EtOAc three times, and the combined layers were dried over Na2SO4. After concentration under reduced pressure, the residue was purified by column chromatography (NH, Hexane/EtOAc=4/1) to yield (1S,4S)-4-(3-pyridyl)-2-cyclopenten-1-ol (1.88 g, 55%) as yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08071591B2
出典データセットuspto-grants-2011_12
ORD IDord-d22fd8b1de6d415ca3aaf9eda8aed6b2
出典メモuspto-grants-2011_12