Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127021Generated: October 26, 2026

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

https://huagongshe.com/reaction/127021

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
ReactantPotassium PermanganateHCID 516875—
ReactantN-(4,5,6,7-Tetrahydrobenzo[b]thiophen-4-yl)acetamideHCID 4976773—
SolventIsopropanolHCID 3776—
ProductAcetamide, N-(4,5,6,7-tetrahydro-7-oxobenzo[b]thien-4-yl)-HCID 10667573.6%

Reaction Conditions

Temperature10 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04254268
Source datasetuspto-grants-1981_03
ORD IDord-2393d935f34849278ec1060f71ea4d4e
Source noteuspto-grants-1981_03