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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 217504Erstellt: 23. Oktober 2026

Sodium Hydroxide → 3-Bromo-5-(trifluoromethyl)benzaldehyde

https://huagongshe.com/de/reaction/217504

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium HydroxideHCID 14798—
EduktTriacetoxyperiodinaneHCID 159087—
Edukt[3-Bromo-5-(trifluoromethyl)phenyl]methanolHCID 29919767—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-Bromo-5-(trifluoromethyl)benzaldehydeHCID 16115438—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A solution of [3-bromo-5-(trifluoromethyl)phenyl]methanol (409 mg, 1.61 mmol) in CH2Cl2 (25 mL) was cooled to 0° C. and then Dess-Martin periodinane (1.02 g, 2.41 mmol) was added. The reaction was stirred at 0° C. for 30 minutes and then warmed to room temperature. After stirring at room temperature for thirty minutes, the reaction was poured into 1N NaOH (25 mL). The mixture was extracted with EtOAc (100 mL), and the organic extracts were washed with 1N NaOH (25 mL), then brine (25 mL), dried over Na2SO4, filtered, and concentrated. Purification by flash chromatography with 25% EtOAc/hexanes afforded 3-bromo-5-(trifluoromethyl)benzaldehyde. Rf=0.60 (25% EtOAc/hexanes). 1H NMR (CDCl3, 500 MHz) δ 10.02 (s, 1H), 8.20 (s, 1H), 8.07 (s, 1H), 8.02 (s, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08193365B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-c8db1d8fd8d745c88b07a88109cc08e0
Quellennotizuspto-grants-2012_06