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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 747866Erstellt: 25. Oktober 2026

Ethanethiol → 7-Hydroxy-4-methyl-3-pyridin-4-yl-chromen-2-one

https://huagongshe.com/reaction/747866

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanethiolHCID 6343—
EduktAluminum bromideHCID 24409—
Edukt7-Methoxy-4-methyl-3-pyridin-4-yl-chromen-2-oneHCID 11659018—
LösungsmittelDichloromethaneHCID 6344—
Produkt7-Hydroxy-4-methyl-3-pyridin-4-yl-chromen-2-oneHCID 135502913—

Reaktionsschritte

To a solution of 7-methoxy-4-methyl-3-pyridin-4-yl-chromen-2-one (600 mg, 2.24 mmoL) in CH2Cl2 (10 mL) at 0° C. was added EtSH (˜1 mL) followed by AlBr3 (6.74 mmoL, 1.80 g). The mixture was slowly warm to room temperature and poured into ice sat. NaHCO3 solution. Extraction was conducted 3× with CH2Cl2. The combined organic layer was washed with brine, dried over anhydrous Na2SO4, filtered and concentrated to give the crude material, which was then purified by silica gel column chromatography using hexanes:ethyl acetate 1:1 as eluent to afford the title product as pale yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07399767B2
Quelldatensatzuspto-grants-2008_07
ORD IDord-2f8b5397725240e8bf29bd29c8541eb3
Quellennotizuspto-grants-2008_07