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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2283262Erstellt: 24. Oktober 2026

Diethyl chlorophosphate → 1-Bromo-4-[(E)-2-ethoxysulfonylethenyl]benzene

https://huagongshe.com/de/reaction/2283262

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl chlorophosphateHCID 13139—
Edukt4-BromobenzaldehydeHCID 70741—
Edukt1-PropanesulfonateHCID 4431756—
EduktButyllithiumHCID 178418339—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-Bromo-4-[(E)-2-ethoxysulfonylethenyl]benzeneHCID 8663200264%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

n-Butyllithium (59.0 mL, 1.6M solution in hexanes) was added dropwise during 25 min to a solution of ethylmethanesulfonate (9.1 mL, 86 mmol) in THF (200 mL) at −78° C. The reaction mixture was stirred for 15 min then diethyl chlorophosphate (7.2 ml, 50 mmol) was added dropwise. The solution was stirred at −78° C. for 30 min, allowed to warm to 0° C. and then cooled to −78° C. again. 4-Bromobenzaldehyde (9.2 g, 50 mmol) in THF (50 mL) was then added dropwise during 15 minutes and the resulting mixture was then allowed to slowly reach RT and stirred overnight. Water (20 mL) was added to the mixture and the reaction was concentrated in vacuo. The residue was extracted with diethyl ether and the combined organic extracts were washed with aqueous saturated sodium chloride, dried over magnesium sulfate, filtered and the solvent was evaporated in vacuo. Purification by column chromatography, using 15% ethyl acetate/hexanes as the eluent, afforded the title compound (9.3 g, 64%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09145380B2
Quelldatensatzuspto-grants-2015_09
ORD IDord-e6e13d12bb50468b8e062189a5b6d9dd
Quellennotizuspto-grants-2015_09