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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | bis-(N-methyl-N-fluorocarbonylamino)sulfide | HCID 12897270 | — |
| Reactant | 5-Oxo-2,2,4-trimethyl-3-thiazoline oxime | HCID 136229054 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-oxo-2,2,4-trimethyl-3-thiazoline O-[N-(N-methylfluoroformamidothio)-N-methylcarbamoyl]oxime | HCID 53886730 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04514566 |
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| Source dataset | uspto-grants-1985_04 |
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| ORD ID | ord-2f5c88dbb8f24077b1f30030dd6ef7ad |
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| Source note | uspto-grants-1985_04 |
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