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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 655161Erstellt: 24. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-IodopyridineHCID 70714—
Eduktrac-(1R,4S)-4-hydroxycyclopent-2-en-1-yl acetateHCID 10154103—
EduktHCID 178418546HCID 178418546—
EduktHCID 178418918HCID 178418918—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelAmmonium ChlorideHCID 25517—
Produkt(1S,4S)-4-(3-pyridyl)-2-cyclopenten-1-olHCID 5948612155,3%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08071591B2
Quelldatensatzuspto-grants-2011_12
ORD IDord-d22fd8b1de6d415ca3aaf9eda8aed6b2
Quellennotizuspto-grants-2011_12