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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 349033Erstellt: 25. Oktober 2026

Potassium Hydroxide → 1-Butyl-1,2,3,4-tetrahydroquinoline-7-carboxylic acid

https://huagongshe.com/reaction/349033

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium HydroxideHCID 14797—
EduktMethyl 1-butyl-1,2,3,4-tetrahydroquinoline-7-carboxylateHCID 21086131—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
Produkt1-Butyl-1,2,3,4-tetrahydroquinoline-7-carboxylic acidHCID 2108516594,6%

Reaktionsschritte

To a stirred solution of methyl 1-butyl-1,2,3,4-tetrahydroquinoline-7-carboxylate (156 mg, 0.63 mmol) in methanol (1.3 mL) was added potassium hydroxide (6.3 mL of a 1 M solution in water, 6.3 mmol). The reaction mixture was stirred at room temperature for 48 h and concentrated under reduced pressure. The residue was diluted with water and washed with ethyl acetate. The aqueous layer was acidified to pH 4 with 1 N hydrochloric acid and extracted with chloroform (4×100 mL). The combined organic extracts were dried (sodium sulfate), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica, 1:9 methanol/chloroform) afforded 1-butyl-1,2,3,4-tetrahydroquinoline-7-carboxylic acid (139 mg): ESI MS m/z 234 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07176242B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-47a1a3aedd774fc1a74f03771b792dea
Quellennotizuspto-grants-2007_02