Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1981374Generated: November 2, 2026

Triethylamine → 5-oxo-2,2,4-trimethyl-3-thiazoline O-[N-(N-methylfluoroformamidothio)-N-methylcarbamoyl]oxime

https://huagongshe.com/reaction/1981374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactantbis-(N-methyl-N-fluorocarbonylamino)sulfideHCID 12897270—
Reactant5-Oxo-2,2,4-trimethyl-3-thiazoline oximeHCID 136229054—
SolventTolueneHCID 1140—
Product5-oxo-2,2,4-trimethyl-3-thiazoline O-[N-(N-methylfluoroformamidothio)-N-methylcarbamoyl]oximeHCID 53886730—

Reaction Conditions

Temperature-50 °C

Reaction Steps

8.3 ml of triethylamine are added dropwise to a suspension of 8.59 g of 5-oxo-2,2,4-trimethyl-3-thiazoline oxime in a solution of 10.0 g of bis-(N-methyl-N-fluorocarbonylamino)sulfide in 100 ml of absolute toluene, cooled to -50° C. The resulting clear solution is allowed to warm slowly to 0° C. during 11/2 hours, during which time a crystalline product is precipitated. The reaction mixture is poured into ice-cold brine and extracted with ethyl acetate. After drying the organic phase over anhydrous sodium sulfate and evaporating it, the resulting residue is purified by chromatography on silica gel (eluent:ethyl acetate/n-hexane 1:1). Crystallization from ethyl acetate/n-hexane yields 5-oxo-2,2,4-trimethyl-3-thiazoline O-[N-(N-methylfluoroformamidothio)-N-methylcarbamoyl]oxime, m.p. 77°-79° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04514566
Source datasetuspto-grants-1985_04
ORD IDord-2f5c88dbb8f24077b1f30030dd6ef7ad
Source noteuspto-grants-1985_04