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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1012652Erstellt: 27. Oktober 2026

Boron tribromide → 2-Fluoro-5-hydroxybenzaldehyde

https://huagongshe.com/reaction/1012652

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBoron tribromideHCID 25134—
Edukt2-Fluoro-5-methoxybenzaldehydeHCID 2734872—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-Fluoro-5-hydroxybenzaldehydeHCID 587247—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

2-Fluoro-5-methoxy-benzaldehyde (4 g, 26 mmol) was dissolved in dry DCM (25 mL) under an argon atmosphere, cooled to 0° C. and slowly added boron tribromide (26 mL, 1.0 M in DCM, 26 mmol). On completion of the addition the reaction mixture was allowed to warm to RT and stirred for 16 h under an argon atmosphere. The reaction was carefully quenched with water (10 mL), added sat. NaHCO3 (30 mL), then shaken and the layers were separated. The aqueous phase was extracted with two more portions of DCM. The organic phases were combined, extracted with 2N NaOH (2×100 mL). The combined NaOH-phases were acidified with HCl (konc.) and extracted with DCM (4×150 mL). The organic phases were combined, dried (MgSO4), filtered, and concentrated in vacuo to afford the crude product. Purified by chromatography using EtOAc/petroleum ether (40-60)(v:v=1:5) as the eluent, affording the title compound as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07977387B2
Quelldatensatzuspto-grants-2011_07
ORD IDord-5776025649f947aa8bdc7702642d95e3
Quellennotizuspto-grants-2011_07