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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 38424Erstellt: 23. Oktober 2026

Tetrahydrofuran → 1-(Thiophen-3-yl)butan-1-one

https://huagongshe.com/de/reaction/38424

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
Edukt3-BromothiopheneHCID 13383—
EduktN-Methoxy-N-methylbutyramideHCID 13704543—
LösungsmittelPropan-2-one--water (1/1)HCID 18366337—
Produkt1-(Thiophen-3-yl)butan-1-oneHCID 2015804364%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

3-Bromothiophene (11 g, 67 mmol) dissolved in hexanes (110 ml) was cooled to −20 C in acetone/water bath, and n-Bu Li (28 ml, 71 mmol, 2.5 N solution in hexanes) was added slowly, over 10 min, then stirred 10 min at −20 C. THF was added (10 ml) over 5 min with rapid stirring. Precipitate formed after about ⅔ of addition. After adding all of the THF, the reaction mixture was stirred 20 min at −20 C, then 20 ml hexanes was added and the reaction mixture was allowed to warm to zero degrees C. N-Methoxy-N-methyl-butyramide (9.29 g, 71 mmol) dissolved in 20 ml hexanes was added via cannula over 5 minutes, and the reaction mixture was stirred at zero degrees C. for 1.5 hours. The reaction mixture was quenched with water, then 1 N HCl (75 ml), extracted twice with ether, washed 1 N HCl, brine, and dried over magnesium sulfate. Solvent was removed under reduced pressure to give an oil, which was chromatographed by flash chromatography (5% EtOAc/hexanes) to give 6.7 g, 64% of 1-Thiophen-3-yl-butan-1-one as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524725B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-48b632c521d24975b6532861b06c9968
Quellennotizuspto-grants-2013_09