Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 327398Erstellt: 25. Oktober 2026

Dihydrobenzofuran → 5-[3-(1-Acetylpiperidin-4-yl)-1-oxopropyl]-2,3-dihydrobenzofuran

https://huagongshe.com/reaction/327398

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDihydrobenzofuranHCID 10329—
EduktAluminum(III) ChlorideHCID 6451240—
Edukt3-(1-Acetyl-4-piperidinyl)propionyl chlorideHCID 10465951—
Lösungsmittel1,2-DichloroethaneHCID 11—
Produkt5-[3-(1-Acetylpiperidin-4-yl)-1-oxopropyl]-2,3-dihydrobenzofuranHCID 1910846478%

Reaktionsschritte

To 200 ml of 1,2-dichloroethane were added 9.65 g (44 mmol) of 3-(1-acetylpiperidin-4-yl)propionic acid chloride and 10.65 g (89 mmol), of 2,3-dihydrobenzofuran. To the mixture was added 12.82 g (96 mmol) of aluminum chloride in limited amounts, then the mixture was stirred for 3 hours at room temperature. The reaction mixture was poured into ice-water, which was subjected to extraction with methylene chloride. Organic layers were combined and washed with water and dried over anhydrous sodium sulfate, followed by distilling off the solvent. The residue was purified by means of a silica gel column chromatography (ethyl acetate) to give 10.47 g (78%) of 5-[3-(1-acetylpiperidin-4-yl)-1-oxopropyl]-2,3-dihydrobenzofuran. Recrystallization from methylene chloride--diethyl ether gave colorless needles, m.p. 93°-95° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05273974
Quelldatensatzuspto-grants-1993_12
ORD IDord-dc431fe2c63742daafd4a5bb569f15bc
Quellennotizuspto-grants-1993_12