HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2255950Generated: October 31, 2026
Water → 4,5,6,7-tetrahydro-4-(4-nitrobenzoyl)-8H-thieno[3,2-b]azepin-8-one
https://huagongshe.com/reaction/2255950
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Reactant | Potassium Permanganate | HCID 516875 | — |
| Reactant | 4-(4-Nitrobenzoyl)-5,6,7,8-tetrahydro-4H-thieno[3,2-b]azepine | HCID 15369398 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4,5,6,7-tetrahydro-4-(4-nitrobenzoyl)-8H-thieno[3,2-b]azepin-8-one | HCID 19699065 | 60.5% |
Reaction Steps
To a solution of 9.0 g of 4-(4-nitrobenzoyl)-5,6,7,8-tetrahydro-4H-thieno[3,2-b]azepine in 713 ml of acetone is added 6.74 g of MgSO4 and 351 ml of water followed by 8.2 g of KMnO4 and heating at 70° C. for 18 hours. Another 6.24 g of MgSO4 and 8.2 g of KMnO4 is added and heating continued at170° C. for 8 hours. An reaction mixture is filtered through diatomaceous earth and the cake washed with acetone and 500 ml of methylene chloride. The combined filtrates are evaporated in vacuo to a residue which is washed with water and air dried to give 5.7 g of a solids The solid is crystallized from ethyl acetate to give 5.1 g of off white solid, m.p. 184°-186° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05654297 |
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| Source dataset | uspto-grants-1997_08 |
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| ORD ID | ord-528a6a4078c642d5bf6f69d013561b08 |
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| Source note | uspto-grants-1997_08 |
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