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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2175898Erstellt: 26. Oktober 2026

Sulfuric acid magnesium salt (1:1) → 6,7-Dihydro-5H-cyclopenta[b]pyridin-5-ol

https://huagongshe.com/reaction/2175898

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric acid magnesium salt (1:1)HCID 24083—
EduktPyrindanHCID 68292—
EduktPotassium PermanganateHCID 516875—
EduktSodium borohydrideHCID 4311764—
LösungsmittelAcetoneHCID 180—
LösungsmittelWaterHCID 962—
LösungsmittelIsopropanolHCID 3776—
Produkt6,7-Dihydro-5H-cyclopenta[b]pyridin-5-olHCID 51064090—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

To a solution of 6,7-dihydro-5H-cyclopenta[b]pyridine (5.0 g, 42 mmol) and MgSO4 (10 g, 84 mmol) in acetone (250 mL) was added a solution of KMnO4 (13 g, 84 mmol) in water (500 mL) at 60 degrees. The mixture was allowed to stir for 30 minutes at 60° C. IPA was slowly added to quench excess KMnO4. The reaction was filtered through a pad of Celite. The filtrate was concentrated under reduced pressure and pumped on a high vacuum pump to ensure complete removal of water. The residue was dissolved in ethanol (200 mL), and cooled with an ice bath. To this solution was slowly added NaBH4 (3.2 g, 84 mmol). When TLC showed complete reduction, water was added to quench excess NaBH4. Ethanol was removed on a rotavapor. The crude material was dissolved in EtOAc, washed with aq. NaHCO3, dried over sodium sulfate, and purified by MPLC (MeOH-DCM: 0-7%). The title compound was collected. LC-MS (IE, m/z): 136 [M+1]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09062070B2
Quelldatensatzuspto-grants-2015_06
ORD IDord-a897840c1150464f9b99acb7c65261e4
Quellennotizuspto-grants-2015_06