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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dihydrobenzofuran | HCID 10329 | — |
| Edukt | Aluminum(III) Chloride | HCID 6451240 | — |
| Edukt | 3-(1-Acetyl-4-piperidinyl)propionyl chloride | HCID 10465951 | — |
| Lösungsmittel | 1,2-Dichloroethane | HCID 11 | — |
| Produkt | 5-[3-(1-Acetylpiperidin-4-yl)-1-oxopropyl]-2,3-dihydrobenzofuran | HCID 19108464 | 78% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05273974 |
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| Quelldatensatz | uspto-grants-1993_12 |
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| ORD ID | ord-dc431fe2c63742daafd4a5bb569f15bc |
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| Quellennotiz | uspto-grants-1993_12 |
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