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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 234255Erstellt: 23. Oktober 2026

Water → (Z)-5-Acetylamino-2,4,6,7-tetramethyl-2-styryl-2,3-dihydrobenzofuran

https://huagongshe.com/de/reaction/234255

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktHCID 19078578HCID 19078578—
EduktHCID 178418244HCID 178418244—
KatalysatorBenzyltriphenylphosphonium chlorideHCID 70671—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(Z)-5-Acetylamino-2,4,6,7-tetramethyl-2-styryl-2,3-dihydrobenzofuranHCID 6767145077,2%

Reaktionsbedingungen

Temperatur-20 °C

Reaktionsschritte

A suspension of benzyltriphenylphosphonium chloride (0.7 g, 1.8 mmol) in tetrahydrofuran (10 ml) was cooled to -20° C. and n-butyllithium hexane solution (1.6M, 1.12 ml, 1.8 mmol) was added dropwise. The reaction mixture was stirred for 30 minutes and then a solution of 5-acetylamino-2-formyl-2,4,6,7-tetramethyl-2,3-dihydrobenzofuran (0.45 g, 1.7 mmol) in tetrahydrofuran (5 ml) was added. The reaction mixture was stirred at room temperature for additional 30 minutes. Water was added to the reaction mixture and the product was extracted with ethyl acetate. The extract was washed with water, dried and then concentrated. The residue was purified by column chromatography on silica gel (isopropyl ether-ethyl acetate, 1:1) to obtain the desired compound (0.44 g, yield: 76.2%) as oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05594154
Quelldatensatzuspto-grants-1997_01
ORD IDord-58df597f495940dda9f2b60e6efab7b3
Quellennotizuspto-grants-1997_01