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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1501075Erstellt: 26. Oktober 2026

Salicylaldehyde → 2-(2,2-Dibromovinyl)phenol

https://huagongshe.com/reaction/1501075

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSalicylaldehydeHCID 6998—
EduktTriethylamineHCID 8471—
EduktCarbon tetrabromideHCID 11205—
EduktTriphenylphosphineHCID 11776—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-(2,2-Dibromovinyl)phenolHCID 999367277,5%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of triphenylphosphine (10.5 g, 40 mmol), carbon tetrabromide (6.6 g, 20 mmol) and triethylamine (3.0 g, 30 mmol) in dichloromethane (10 mL) was added 2-hydroxy-benzaldehyde (1.62 g, 13 mmol), and the mixture temperature was maintained at around 0° C. during the addition. After the addition was completed, the reaction mixture was stirred at room temperature for 1 hour. After the reaction, the mixture was poured into water (200 mL). And then the mixture was extracted with ethyl acetate (200 mL), washed with water (200 mL). The organic phase was dried over anhydrous sodium sulfate, and then filtered. The filtrate was concentrated and the residue was purified by column chromatography (silica gel, ethyl acetate/petroleum ether=1:5) to give the pure product 2-(2,2-dibromovinyl)phenol as a pink solid (2.8 g, 76%). LRMS (M−H)−: calcd 275.9. found 275.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09206128B2
Quelldatensatzuspto-grants-2015_12
ORD IDord-6807387dc472492eab554fd2f239255e
Quellennotizuspto-grants-2015_12