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HRID 44177Erstellt: 23. Oktober 2026

Hydrochloric Acid → 1,2,6,7-tetrahydro-5H-pyrido[3,2,1-ij]quinolin-3-one

https://huagongshe.com/de/reaction/44177

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSodium ChlorideHCID 5234—
Edukt3-Chloropropionyl chlorideHCID 69364—
Edukt1,2,3,4-TetrahydroquinolineHCID 69460—
EduktAluminum(III) ChlorideHCID 6451240—
LösungsmittelAcetoneHCID 180—
LösungsmittelWaterHCID 962—
Produkt1,2,6,7-tetrahydro-5H-pyrido[3,2,1-ij]quinolin-3-oneHCID 1369456488%

Reaktionsschritte

A solution of 3-chloropropanoyl chloride (9.1 ml, 95.0 mmol) in 20 ml dry acetone was added dropwise to a solution of 1,2,3,4-tetrahydroquinoline (26.6 g, 0.20 mol) in 80 ml dry acetone and the mixture was refluxed for 1 h. After cooling to ambient temperature the solution was poured into 500 ml stirred 2N HCl and extracted with ethyl acetate (3×150 ml). After washing with 1N HCl and brine and drying over MgSO4 the solvent was removed under reduced pressure and the crude product was obtained as a pale yellow solid. This was added portionwise to a molten mixture of AlCl3 (60.0 g, 0.45 mol) and NaCl (17.5 g, 300 mmol) at 150° C. and stirred for additional 30 minutes. On cooling, excess aluminum chloride was decomposed by the addition of a chilled mixture of 20 ml concentrated hydrochloric acid and 500 ml water. Extraction with ethyl acetate (3×200 ml), followed by drying over MgSO4 and removal of the solvent gave 1,2,6,7-tetrahydro-5H-pyrido[3,2,1-ij]quinolin-3-one (15.6 g, 83.3 mmol, 88%) as a yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08541404B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-ac8487d98fac4d3f809c9f75df60e941
Quellennotizuspto-grants-2013_09