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

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.

1. stirringAfter stirring
2. waitwas continued at 3° C. for 30 min, to the resulting solution
3. stirringThe whole mixture was stirred at the room temperature for 2 h
4. extractionThe products were extracted with EtOAc three times
5. dry with materialthe combined layers were dried over Na2SO4
6. concentrationAfter concentration under reduced pressure
7. customthe residue was purified by column chromatography (NH, Hexane/EtOAc=4/1)

ORD-Eintrag

ord-d22fd8b1de6d415ca3aaf9eda8aed6b2

Quelldatensatz

uspto-grants-2011_12

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08071591B2