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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 569163Erstellt: 26. Oktober 2026

Water → 3-[p-(3-Chloropropionyl)benzyl]pyridine

https://huagongshe.com/reaction/569163

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt3-Chloropropionyl chlorideHCID 69364—
EduktAluminum(III) ChlorideHCID 6451240—
Edukt3-Benzylpyridine hydrochlorideHCID 12210545—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-[p-(3-Chloropropionyl)benzyl]pyridineHCID 2014863786,6%

Reaktionsschritte

In 15 ml of methylene chloride was suspended 8.1 g of anhydrous aluminum chloride, and 3.0 ml of 3-chloropropionyl chloride was added to the suspension with ice-cooling, after which 5.0 g of 3-benzylpyridine hydrochloride was added in small portions to the resulting mixture over 30 minutes. The resulting mixture was subjected to reaction at room temperature for one hour, and then the reaction mixture was added to 30 ml of iced water. The crystals thus precipitated were collected by filtration, and suspended in a mixture of 50 ml of ethyl acetate and 30 ml of water, after which the resulting suspension was neutralized with sodium hydrogencarbonate with ice-cooling. Insolubles were removed by filtration, and the organic layer of the filtrate was separated, washed with 10 ml of a saturated aqueous sodium chloride solution, and then dried over anhydrous magnesium sulfate, after which the solvent was removed by distillation under reduced pressure to obtain 5.5 g (yield 86.6%) of pale yellow, oily 3-[p-(3-chloropropionyl)benzyl]pyridine.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04731370
Quelldatensatzuspto-grants-1988_03
ORD IDord-f09894232a584e41b2b54586fe417ef3
Quellennotizuspto-grants-1988_03