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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1876997Erstellt: 25. Oktober 2026

3-Heptanone → Ethyl 2-ethyl-5-(1-ethyl-1-hydroxypropyl)thiophene-3-carboxylate

https://huagongshe.com/reaction/1876997

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-HeptanoneHCID 7802—
EduktAmmonium ChlorideHCID 25517—
EduktEthyl 5-bromo-2-ethylthiophene-3-carboxylateHCID 68515411—
EduktHCID 178420663HCID 178420663—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktEthyl 2-ethyl-5-(1-ethyl-1-hydroxypropyl)thiophene-3-carboxylateHCID 68512433—

Reaktionsschritte

To a solution of ethyl 5-bromo-2-ethylthiophene-3-carboxylate (3.00 g) synthesized in Example 69 (4) in tetrahydrofuran (50 mL) was added dropwise 1.0M isopropylmagnesium bromide-tetrahydrofuran solution (13.7 mL) at −45° C. After stirring under an argon atmosphere for 1 hr, 1.0M isopropylmagnesium bromide-tetrahydrofuran solution (13.7 mL) was added dropwise, and the mixture was stirred for 1 hr. 3-Heptanone (6.04 mL) was added dropwise, and the mixture was stirred at −45° C. for 1 hr, and at room temperature for 1 hr. Saturated aqueous ammonium chloride solution was added to quench the reaction, and the mixture was extracted with ethyl acetate. The extract was washed with brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=3:17, volume ratio) to give the title compound (3.06 g, quantitative) as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08309580B2
Quelldatensatzuspto-grants-2012_11
ORD IDord-888730f20d674d77a67762f5c23b3b4f
Quellennotizuspto-grants-2012_11