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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 266094Erstellt: 26. Oktober 2026

Sodium borohydride → alpha-[1-[2-(4-Methoxyphenyl)ethyl]-4-piperidinyl]-2-benzothiazolemethanol

https://huagongshe.com/reaction/266094

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium borohydrideHCID 4311764—
Edukt[2-Benzothiazolyl][1-[2-(4-methoxyphenyl)ethyl]-4-piperidinyl)methanoneHCID 9842862—
LösungsmittelMethanolHCID 887—
Produktalpha-[1-[2-(4-Methoxyphenyl)ethyl]-4-piperidinyl]-2-benzothiazolemethanolHCID 18930333—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Dissolve [2-benzothiazolyl][1-[2-(4-methoxyphenyl)ethyl]-4-piperidinyl]methanone (3.0 g, 7.88 mmol) in methanol (150 mL) and cool to 0° C. Add sodium borohydride (597 mg, 15.77 mmol) and stir for 1.5 hours, adding additional sodium borohydride after 30 minutes. Evaporate the solvent in vacuo and partition the residue between water and methylene chloride. Separate the organic phase, wash with saturated sodium chloride, dry (MgSO4) and evaporate the solvent in vacuo. Purify by recrystallization (ethyl acetate) to give the title compound as white fluffy crystals; mp 127°-129° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05650416
Quelldatensatzuspto-grants-1997_07
ORD IDord-e3d0f09abc84486991f02f7687bec246
Quellennotizuspto-grants-1997_07