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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1391727Erstellt: 27. Oktober 2026

Sodium borohydride → 1-{6-[4-(Trifluoromethyl)phenyl]-2-pyridinyl}-1-pentanol

https://huagongshe.com/reaction/1391727

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium borohydrideHCID 4311764—
Edukt1-{6-[4-(Trifluoromethyl)phenyl]-2-pyridinyl}-1-pentanoneHCID 58629901—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-{6-[4-(Trifluoromethyl)phenyl]-2-pyridinyl}-1-pentanolHCID 5862982299,7%

Reaktionsschritte

A mixture of 1-{6-[4-(trifluoromethyl)phenyl]-2-pyridinyl}-1-pentanone (2.80 g, 9.11 mmol) in THF (61 mL) at 0° C. (ice/water bath) was treated drop-wise with a mixture of sodium borohydride (689 mg, 18.21 mmol) in water (11 mL) over 5-10 minutes. The resulting mixture was stirred at this temperature for 2.5 hours and was then partitioned between EtOAc (200 mL) and water (200 mL) and the layers separated. The aqueous was re-extracted with EtOAc (200 mL) and the combined organic layer washed with brine (250 mL), dried (MgSO4), filtered and reduced. Purification by Biotage™ chromatography (silica) eluting with cyclohexane:EtOAc (gradient 20:1 to 5:1) afforded the title compound as a colourless oil (2.81 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07338960B2
Quelldatensatzuspto-grants-2008_03
ORD IDord-beda19d4626a4e8c874d260255c78966
Quellennotizuspto-grants-2008_03