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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 24024Erstellt: 24. Oktober 2026

Piperonal → 5-(2,2-Dibromo-vinyl)-benzo[1,3]dioxole

https://huagongshe.com/de/reaction/24024

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPiperonalHCID 8438—
EduktCarbon tetrabromideHCID 11205—
EduktTriphenylphosphineHCID 11776—
LösungsmittelDichloromethaneHCID 6344—
Produkt5-(2,2-Dibromo-vinyl)-benzo[1,3]dioxoleHCID 1096876474%

Reaktionsschritte

To a solution of piperonal (4.5 g, 30 mmol) and triphenylphosphine (24 g, 90 mmol) in DCM (120 mL) in an ice-water bath was added a solution of carbontetrabromide (15 g, 45 mmol) over a 10 minutes period. After the addition completed, the ice-water bath was removed, the reaction stirred at ambient temperature for 2 h, and then quenched with saturated NaHCO3. Aqueous was separated, and extracted with dichloromethane (2 times). The organic layers were combined, dried over Na2SO4, filtered, and concentrated to give a redish colored residue, that was filtered through a short path silica gel plug, eluting with DCM/hexane (10% to 20%). Concentration of the filtrate gave the title compound (6.5 g, 74% yield) as a pale yellow liquid. 1H NMR (CDCl3) δ 7.36 (s, 1H), 7.18 (d, 1H, J=1.6 Hz), 6.95 (dd, 1H, J=1.5, 8.1 Hz), 6.79 (d, 1H, J=8.1 Hz), 5.99 (s, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06855722B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-b1d78607255e4db591db91c514e39db9
Quellennotizuspto-grants-2005_02