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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 127021Erstellt: 24. Oktober 2026

Acetone → Acetamide, N-(4,5,6,7-tetrahydro-7-oxobenzo[b]thien-4-yl)-

https://huagongshe.com/de/reaction/127021

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetoneHCID 180—
EduktSulfuric acid magnesium salt (1:1)HCID 24083—
EduktPotassium PermanganateHCID 516875—
EduktN-(4,5,6,7-Tetrahydrobenzo[b]thiophen-4-yl)acetamideHCID 4976773—
LösungsmittelIsopropanolHCID 3776—
ProduktAcetamide, N-(4,5,6,7-tetrahydro-7-oxobenzo[b]thien-4-yl)-HCID 10667573,6%

Reaktionsbedingungen

Temperatur10 °C

Reaktionsschritte

Acetone (200 ml), N-(4,5,6,7-tetrahydrobenzo[b]-thien-4-yl) acetamide (9.75 g, 0.05 mol) and magnesium sulfate (21.0 g, 0.17 mol) are mixed, stirred and cooled to 10° C. Next, 150 ml of an aqueous potassium permanganate solution (prepared from 21.0 g, 0.133 mol of potassium permanganate and 200 ml of water) is added over 15 minutes to the above mixture, and the whole stirred for 3 hours. After 3 hours reaction time, analysis of the mixture by high pressure liquid chromatography (HPLC) indicates the reaction to be incomplete. The remainder of the above potassium permanganate solution (~50 ml) is added and the reaction mixture stirred for two more hours. Isopropanol (20 ml) is then added, the reaction mixture stirred overnight, and filtered. HPLC analysis of the filtered solution indicates a 73.6% yield of title product, and also the presence of 2% of starting material.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04254268
Quelldatensatzuspto-grants-1981_03
ORD IDord-2393d935f34849278ec1060f71ea4d4e
Quellennotizuspto-grants-1981_03