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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 17060Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/17060

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
PatentnummerUS07737295B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-74f4dd60082d45da8113fa788f74dd72
Quellennotizuspto-grants-2010_06