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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 390630Erstellt: 25. Oktober 2026

Sodium hydride → Ethyl 2-[1-(3-butoxy-4-iodophenyl)meth-(e)-ylidene]butyrate

https://huagongshe.com/reaction/390630

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
EduktAmmonium ChlorideHCID 25517—
EduktEthyl 2-(diethoxyphosphoryl)butanoateHCID 229053—
Edukt3-Butoxy-4-iodobenzaldehydeHCID 59574930—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktEthyl 2-[1-(3-butoxy-4-iodophenyl)meth-(e)-ylidene]butyrateHCID 6895709397%

Reaktionsschritte

A solution of 9 mL (37.8 mmol) of triethyl 2-phosphonobutyrate in 20 mL of tetrahydrofuran is added to a mixture of 1.52 g (37.8 mmol) of sodium hydride in 15 mL of tetrahydrofuran. The reaction medium is stirred for 20 minutes. A solution of 3.83 g (12.6 mmol) of 3-butoxy-4-iodobenzaldehyde (prepared as described in Example 19g) in 15 mL of tetrahydrofuran is then added to the reaction mixture and the reaction medium is stirred at room temperature for 2 hours 30 minutes. The reaction medium is poured into saturated ammonium chloride solution and extracted with ethyl acetate. The organic phases are combined, washed with saturated sodium chloride solution and dried over magnesium sulfate. The solvent is evaporated off and the residue (11.49 g) is purified by chromatography on silica gel eluted with a 95/5 heptane/ethyl acetate mixture. 4.90 g (97%) of ethyl 2-[1-(3-butoxy-4-iodophenyl)meth-(E)-ylidene]butyrate are obtained in the form of a yellow oil that crystallizes.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08383652B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-6012fff6f90741bea1e705721ba92685
Quellennotizuspto-grants-2013_02