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HRID 127020Erstellt: 26. Oktober 2026
Sulfuric acid magnesium salt (1:1) → Acetamide, N-(4,5,6,7-tetrahydro-7-oxobenzo[b]thien-4-yl)-
https://huagongshe.com/reaction/127020
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Edukt | Potassium Permanganate | HCID 516875 | — |
| Edukt | N-(4,5,6,7-Tetrahydrobenzo[b]thiophen-4-yl)acetamide | HCID 4976773 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Produkt | Acetamide, N-(4,5,6,7-tetrahydro-7-oxobenzo[b]thien-4-yl)- | HCID 106675 | — |
Reaktionsschritte
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##
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04254268 |
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| Quelldatensatz | uspto-grants-1981_03 |
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| ORD ID | ord-6c00c335a66b4af2a6d810b1a8eade9b |
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| Quellennotiz | uspto-grants-1981_03 |
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