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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 374002Erstellt: 23. Oktober 2026

Water → HCID 54306210, Verbindung

https://huagongshe.com/de/reaction/374002

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt4-(2-Nitrophenyl)-3-buten-2-oneHCID 140761—
EduktHCID 178418244HCID 178418244—
KatalysatorEthyltriphenylphosphonium iodideHCID 78474—
LösungsmittelDiethyl EtherHCID 3283—
ProduktHCID 54306210HCID 5430621042%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

20.3 g of ethyltriphenylphosphonium iodide was suspended in 160 ml of diethyl ether. Thereto was dropwise added 29.4 ml of 1.5 M n-butyllithium hexane solution, in 2 minutes with stirring at 0° C. Then, the mixture was stirred at 20° C. for 1 hour. To the resulting mixture being maintained at 10°-15° C. was dropwise added a solution of 8.4 g of 4-(2-nitrophenyl)-3-buten-2-one dissolved in 40 ml of diethyl ether, in 30 minutes. The resulting mixture was stirred at 20° C. for 3 hours. Thereto was added 100 ml of water. The organic layer was separated. The aqueous layer was extracted with 100 ml of diethyl ether, and the extract was combined with the previously separated organic layer. The combined solution was washed with an aqueous saturated sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure. The residue was purified by column chromatography (eluant: n-hexane/ethyl acetate=5/1) to obtain 3.8 g (yield: 42%) of 1-(3-methyl-1,3-pentadienyl)-2-nitrobenzene as a light yellow oily material.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05166204
Quelldatensatzuspto-grants-1992_11
ORD IDord-d72a41a053c94a029ecd43037fb1cc66
Quellennotizuspto-grants-1992_11