Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 339080Erstellt: 24. Oktober 2026

Sodium Hydroxide → HCID 70984314, Verbindung

https://huagongshe.com/de/reaction/339080

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium HydroxideHCID 14798—
EduktCrotonaldehydeHCID 447466—
EduktSodium BicarbonateHCID 516892—
Edukt(3-Aminophenyl)acetic acidHCID 571807—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelMethanolHCID 887—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelEthyl AcetateHCID 8857—
ProduktHCID 70984314HCID 70984314—

Reaktionsschritte

2-(3-aminophenyl)acetic acid (11.0 g, 72.8 mmol) was dissolved in 6 N HCl (200 mL) and heated to reflux. (E)-but-2-enal (11.9 mL, 146 mmol) was added dropwise over 10 minutes. The reaction was heated at reflux for 2 hours. After cooling to ambient temperature, the reaction mixture was basified with sodium hydroxide to pH˜12 and ether (100 mL) was added. The aqueous layer was separated, acidified with saturated potassium hydrogen sulfate to pH˜3-4, extracted with 3:1 CHCl3:IPA (3×300 mL), dried (sodium sulfate) and concentrated to give a solid. The solid was dissolved in MeOH (200 mL). The residue was suspended in ethyl acetate (100 mL) and saturated sodium bicarbonate (50 mL). The organic layer was separated, washed with brine, dried (sodium sulfate) and concentrated. The residue obtained was purified by flash chromatography (5:1 DCM:ethyl acetate) to give methyl 2-(2-methylquinolin-7-yl)acetate as a solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08889704B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-95c1fe54fc5149898c8905051a9bb4e6
Quellennotizuspto-grants-2014_11