HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1155640Generated: October 26, 2026
Oxygen → Acetamide, N-(4,5,6,7-tetrahydro-7-oxobenzo[b]thien-4-yl)-
https://huagongshe.com/reaction/1155640
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxygen | HCID 977 | — |
| Reactant | Isobutyric Acid | HCID 6590 | — |
| Reactant | N-(4,5,6,7-Tetrahydrobenzo[b]thiophen-4-yl)acetamide | HCID 4976773 | — |
| Solvent | Water | HCID 962 | — |
| Product | Acetamide, N-(4,5,6,7-tetrahydro-7-oxobenzo[b]thien-4-yl)- | HCID 106675 | 37% |
Reaction Steps
Oxygen is passed into a mixture of N-(4,5,6,7-tetrahydrobenzo[b]thien-4-yl)acetamide (1.0 g; 5.13 m mole), cobaltous acetate (0.25 g; 1.4 m mole), cobaltous bromide tetrahydrate (0.32 g; 1.1 m mole), isobutyric acid (20 ml) and water (0.2 ml) in a sintered glass funnel fitted with a condenser and thermometer, via the stem of the funnel. The dark brown mixture is oxygenated for 100 minutes at room temperature, then heated briefly to 48° C. After 2 hours and 10 minutes, the mixture is reheated to 50° C. and the flow of oxygen is terminated 2 hours later. The mixture is then worked up as described in Example 1 to attain a 37% yield of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04332724 |
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| Source dataset | uspto-grants-1982_06 |
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| ORD ID | ord-bcc2d5ee189e42939b6ab27fa5748507 |
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| Source note | uspto-grants-1982_06 |
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