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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1918538Erstellt: 26. Oktober 2026

3,4-dihydro-2H-pyran → 3-(5-chloro-1H-indol-3-yl)propan-1-ol

https://huagongshe.com/reaction/1918538

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3,4-dihydro-2H-pyranHCID 8080—
EduktHydrazine, (4-chlorophenyl)-, hydrochloride (1:1)HCID 71600—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt3-(5-chloro-1H-indol-3-yl)propan-1-olHCID 1997934764,4%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A mixture of (4-chlorophenyl)hydrazine hydrochloride (5.26 g; 28.50 mmol) and 3,4-dihydro-2H-pyran (2.63 mL; 28.50 mmol) in a mixture of water (9 mL) and dioxane (36 mL) was stirred at 100° C. for 48 hours. After cooling to room temperature the mixture was diluted with ethyl acetate. The aqueous layer was separated and further extracted with ethyl acetate. The combined organic layers were dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel (eluent: 0 to 6% methanol in dichloromethane) to afford 3.85 g (64%) of 3-(5-chloro-1H-indol-3-yl)propan-1-ol as an oily residue.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08618138B2
Quelldatensatzuspto-grants-2013_12
ORD IDord-2784cdb7b2824ccfabe6f728c75089fb
Quellennotizuspto-grants-2013_12