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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 414583Erstellt: 24. Oktober 2026

Sodium hydride → 2-(4-Chlorophenyl)-1-(5'-methyl[2,2'-bithienyl]-5-yl)ethene

https://huagongshe.com/de/reaction/414583

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
EduktDiethyl 4-chlorobenzylphosphonateHCID 99240—
Edukt5-(5-Methylthiophen-2-yl)thiophene-2-carbaldehydeHCID 4987278—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-(4-Chlorophenyl)-1-(5'-methyl[2,2'-bithienyl]-5-yl)etheneHCID 54303521—

Reaktionsschritte

Under a nitrogen atmosphere, 0.12 gram (0.0050 mole) of sodium hydride was added to a stirred solution of 1.2 gram (0.0057 mole) of 5-formyl-5'-methyl[2,2'-bithienyl] and 1.7 gram (0.0064 mole) of diethyl 4-chlorobenzylposphonate in 20 mL of N,N-dimethylformamide. The reaction mixture was stirred at room temperature for about three huurs. Analysis of the reaction mixture by thin layer chromatography indicated starting materials remained. Additional sodium hydride was added, and the mixture was stirred at room temperature for several hours. The reaction mixture was quenched with an aqueous solution saturated with ammonium chloride. This mixture was extracted several times with diethyl ether. The extracts were combined and washed with an aqueous solution saturated with sodium chloride. The washed extract was dried over anhydrous magnesium sulfate and filtered. The filtrate was evaporated under reduced pressure leaving a residue. This residue was purified by column chromatography on silica gel to yield 2-(4-chlorophenyl)-1-(5'-methyl[2,2'-bithienyl]-5-yl)ethene as a solid, m.p. 157°-162° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04792567
Quelldatensatzuspto-grants-1988_12
ORD IDord-dd85b256c9904ba0912b9d199ba67bd7
Quellennotizuspto-grants-1988_12