HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006766Generated: October 31, 2026
Acetamide, 2-bromo-N-butyl-N-methyl- → 2-(acetylthio)-N-butyl-N-methylacetamide
https://huagongshe.com/reaction/1006766
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetamide, 2-bromo-N-butyl-N-methyl- | HCID 10798390 | — |
| Reactant | Potassium ethanethioate | HCID 23670855 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(acetylthio)-N-butyl-N-methylacetamide | HCID 19708694 | 100% |
Reaction Steps
4.16 g of bromo-N-butyl-N-methylacetamide of Preparation B of Example 78, Step A in 1.5 ml of methanol were added to a suspension of 2.28 g of potassium thioacetate in 10 ml of methanol and the mixture was heated for one hour at 40° C. under an argon atmosphere. After evaporation to dryness under reduced pressure, the residue was dissolved with ethyl ether, the insoluble part filtered off and the solution was evaporated to dryness to obtain 4.06 g of oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06790971B1 |
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| Source dataset | uspto-grants-2004_09 |
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| ORD ID | ord-686997355a1c4c90be147b7716837c98 |
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| Source note | uspto-grants-2004_09 |
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