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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 15004Erstellt: 25. Oktober 2026

Allyl bromide → 3-(3-Carboethoxyphenyl)-1-propene

https://huagongshe.com/reaction/15004

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAllyl bromideHCID 7841—
EduktEthyl 3-iodobenzoateHCID 143542—
EduktHCID 178418546HCID 178418546—
EduktHCID 178418918HCID 178418918—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-(3-Carboethoxyphenyl)-1-propeneHCID 1207047968,4%

Reaktionsschritte

A −45° C. solution of ethyl 3-iodobenzoate (2.434 g, 8.8 mmol) in 40 mL THF was treated with i-PrMgCl (4.8 mL, 9.6 mmol, 2 M/ether). After 1 h, allyl bromide (1.6 mL, 18.9 mmol) was added followed by CuCN (79 mg, 0.88 mmol). The reaction was stirred for 1 h and then was quenched by addition of 50 mL saturated NH4Cl solution. Water (30 mL) was added and the resulting mixture was extracted with ethyl acetate (3×50 mL). The combined ethyl acetate solution was dried (MgSO4), filtered and evaporated. Purification by flash chromatography on silica gel (5% ethyl acetate/hexanes→10%) gave compound 7 (1.145 g, 68%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07732443B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-5d81dabb02cf41668ac8b0e9abad9b2e
Quellennotizuspto-grants-2010_06