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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2779Erstellt: 23. Oktober 2026

5-Bromo-2-fluorobenzaldehyde → (5-Bromo-2-fluorophenyl)methanol

https://huagongshe.com/de/reaction/2779

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-Bromo-2-fluorobenzaldehydeHCID 736327—
EduktSodium borohydrideHCID 4311764—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(5-Bromo-2-fluorophenyl)methanolHCID 277335297,7%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 5-bromo-2-fluoro-benzaldehyde (6.10 g, 30.0 mmol) in 30 mL of THF at 0° C. is added 5 mL of sodium borohydride (2.0M solution in triglyme, 10.0 mmol). The reaction mixture is stirred at 0° C. for 25 min and then quenched by the addition of 1N HCl. The mixture is diluted with EtOAc and the layers are separated. The organic layer is washed with H2O and saturated NaCl. The organic layer is dried over MgSO4, filtered and concentrated. The crude product is purified by column chromatography eluting with 15% EtOAc/hexanes to afford the title compound (6.00 g, 29.3 mmol).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05731315
Quelldatensatzuspto-grants-1998_03
ORD IDord-dfa8e518af0e4946b9f86e5f4d0e8666
Quellennotizuspto-grants-1998_03