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HRID 127020作成日:2026年10月27日

Sulfuric acid magnesium salt (1:1) → Acetamide, N-(4,5,6,7-tetrahydro-7-oxobenzo[b]thien-4-yl)-

https://huagongshe.com/reaction/127020

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfuric acid magnesium salt (1:1)HCID 24083—
反応物Potassium PermanganateHCID 516875—
反応物N-(4,5,6,7-Tetrahydrobenzo[b]thiophen-4-yl)acetamideHCID 4976773—
溶媒AcetoneHCID 180—
生成物Acetamide, N-(4,5,6,7-tetrahydro-7-oxobenzo[b]thien-4-yl)-HCID 106675—

反応手順

One molar equivalent of N-(4,5,6,7-tetrahydrobenzo[b]thien-4-yl)acetamide is oxidized in aqueous acetone at 10° C. to 15° C. with 2.66 moles of potassium permanganate in the pH range of 7 to 9 in the presence of magnesium sulfate buffer for a period of time from about 3 to 5 hours to afford N-(4,5,6,7-tetrahydro-7-oxobenzo[b]thien-4-yl)acetamide. The thus-obtained oxo-acetamide is hydrolyzed in aqueous hydrochloric acid to the corresponding amine. This amine is then reacted with sodium or potassium cyanate in an aqueous medium at about pH 6.5, and at a temperature of about 60° C. to 65° C., to afford the animal growth-promoting 4,5,6,7-tetrahydro-7-oxobenzo[b]thien-4-ylurea of formula (A). Oxidation of 4,5,6,7-tetrahydrobenzo[b]thien-4-ylurea under reaction conditions, similar to those described above, also affords the aforesaid urea of formula (A). The above reaction sequence may be graphically illustrated as follows: ##STR10##

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04254268
出典データセットuspto-grants-1981_03
ORD IDord-6c00c335a66b4af2a6d810b1a8eade9b
出典メモuspto-grants-1981_03