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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 441053Erstellt: 26. Oktober 2026

Methyl iodide → 5,7-Bis(methoxymethoxy)-2-methylthiochromone

https://huagongshe.com/reaction/441053

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
EduktCarbon DisulfideHCID 6348—
Edukt18-Crown-6HCID 28557—
EduktPotassium hydrideHCID 82127—
Edukt1-[2-Hydroxy-4,6-bis(methoxymethoxy)phenyl]ethanoneHCID 10879697—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt5,7-Bis(methoxymethoxy)-2-methylthiochromoneHCID 5708550791,6%

Reaktionsschritte

Under cooling on ice, potassium hydride (0.5 ml of 35% mineral oil) was suspended in 2 ml THF. 2 ml of 126 mg of 2'-hydroxy-4',6'-bis(methoxymethoxy)acetophenone (0.492 mmol) and 130 mg of 18-crown-6 (0.492 mmol) in THF was added dropwise to the above suspension, and the mixture was stirred for 1 hour. After addition of 0.89 ml of carbon disulfide (14.76 mmol), the solution was stirred for 20 hours at room temperature. Then, 0.5 ml of methyl iodide was added thereto, and the solution was stirred for 30 min. After water was slowly added thereto, the reaction solution was extracted twice with ether, and the organic layer was washed with saturated NaCl water and then dried over sodium sulfate anhydride. The solvent was distilled off and the resulting crude product was washed with hexane, to give 133.5 mg of 5,7-bis(methoxymethoxy)-2-methylthiochromone (87% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05521216
Quelldatensatzuspto-grants-1996_05
ORD IDord-81be17509c404bde932adfb2225d6ac0
Quellennotizuspto-grants-1996_05