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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2266170Erstellt: 26. Oktober 2026

Acetone → 2-Bromo-1-thiophen-3-yl-butan-1-one

https://huagongshe.com/reaction/2266170

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetoneHCID 180—
Edukttert-ButanolHCID 6386—
Edukt2-Bromo-1-thiophen-3-yl-butan-1-oneHCID 59598618—
EduktHCID 178461630HCID 178461630—
LösungsmittelBenzeneHCID 241—
Produkt2-Bromo-1-thiophen-3-yl-butan-1-oneHCID 59598618—
Produkt5-Thiophen-3-yl-heptane-2,4-dioneHCID 59598638—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

EtMgBr (6.69 ml, 13 mmol, 2 M in ethyl ether) in benzene (10 ml) was cooled to zero degrees C, and tBuOH (1.28 ml, 13 mmol) was slowly added. The reaction mixture was stirred at zero degrees C for 5 minutes, then acetone (530 ul, 7 mmol) was added, followed by a solution of 2-Bromo-1-thiophen-3-yl-butan-1-one (1.3 g, 6 mmol) in 3 ml benzene via cannula. The reaction mixture was heated to reflux for 1 hour, and acetone (250 ul) was added. The reaction mixture was heated 2 hours more at reflux. The reaction was cooled, quenched with 1 N HCl (10 ml), extracted three times with diethyl ether, washed brine, and dried over magnesium sulfate. The solvent was removed in vacuo and the residue chromatographed (5% ethyl acetate/hexanes) to give 247 mg of 2-Bromo-1-thiophen-3-yl-butan-1-one starting material and 520 mg of 5-Thiophen-3-yl-heptane-2,4-dione, 44% .

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07858632B2
Quelldatensatzuspto-grants-2010_12
ORD IDord-ccbfb89603834a1a90ac0f1bafeaa854
Quellennotizuspto-grants-2010_12