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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726113Generated: October 29, 2026

Acetamide, 2-bromo-N-butyl-N-methyl- → 2-(acetylthio)-N-butyl-N-methylacetamide

https://huagongshe.com/reaction/726113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetamide, 2-bromo-N-butyl-N-methyl-HCID 10798390—
ReactantPotassium ethanethioateHCID 23670855—
SolventMethanolHCID 887—
Product2-(acetylthio)-N-butyl-N-methylacetamideHCID 19708694100%

Reaction Conditions

Temperature40 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05707982
Source datasetuspto-grants-1998_01
ORD IDord-99a1a93eaf454df29261b73484e74e28
Source noteuspto-grants-1998_01