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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 127020생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/127020

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric acid magnesium salt (1:1)HCID 24083—
반응물Potassium PermanganateHCID 516875—
반응물N-(4,5,6,7-Tetrahydrobenzo[b]thiophen-4-yl)acetamideHCID 4976773—
용매AcetoneHCID 180—
생성물Acetamide, N-(4,5,6,7-tetrahydro-7-oxobenzo[b]thien-4-yl)-HCID 106675—

반응 단계

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##

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04254268
출처 데이터셋uspto-grants-1981_03
ORD IDord-6c00c335a66b4af2a6d810b1a8eade9b
출처 메모uspto-grants-1981_03