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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1981372Generated: November 1, 2026

Potassium Carbonate → 5-oxo-2,2,4-trimethyl-3-thiazoline O-[N-(di-n-butylaminosulphenyl)-N-methylcarbamoyl]oxime

https://huagongshe.com/reaction/1981372

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantN-(di-n-butylaminosulfenyl)-N-fluorocarbonyl-N-methylamineHCID 12799219—
Reactant5-Oxo-2,2,4-trimethyl-3-thiazoline oximeHCID 136229054—
SolventAcetonitrileHCID 6342—
Product5-oxo-2,2,4-trimethyl-3-thiazoline O-[N-(di-n-butylaminosulphenyl)-N-methylcarbamoyl]oximeHCID 54502540—

Reaction Steps

3.0 g (0.019 mol) of 5-oxo-2,2,4-trimethyl-3-thiazoline oxime are suspended in 10 ml of absolute acetonitrile. To the suspension at 0° C. there are successively added 5.5 g of anhydrous potassium carbonate and, dropwise, a solution of 4.52 g of N-(di-n-butylaminosulphenyl)-N-methylcarbamoyl fluoride in 10 ml of absolute acetonitrile. The reaction mixture is allowed to stir well at room temperature for 20 hours. Subsequently, the precipitated potassium salt is filtered off, and the filtrate is evaporated. Chromatography of the crude oily product on silica gel with ethyl acetate/toluene (1:3) as the eluent yields 5-oxo-2,2,4-trimethyl-3-thiazoline O-[N-(di-n-butylaminosulphenyl)-N-methylcarbamoyl]oxime, nD20 1.5200.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04514566
Source datasetuspto-grants-1985_04
ORD IDord-bf1d9ff86c1045608c73b762138fb7ee
Source noteuspto-grants-1985_04