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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1981369Generated: November 2, 2026

Methyl Isocyanate → 5-oxo-2,2,4-trimethyl-3-thiazoline O-(methylcarbamoyl) oxime

https://huagongshe.com/reaction/1981369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl IsocyanateHCID 12228—
Reactant5-Oxo-2,2,4-trimethyl-3-thiazoline oximeHCID 136229054—
CatalystTriethylamineHCID 8471—
SolventChloroformHCID 6212—
Product5-oxo-2,2,4-trimethyl-3-thiazoline O-(methylcarbamoyl) oximeHCID 53689904—

Reaction Steps

20.0 g (0.126 mol) of 5-oxo-2,2,4-trimethyl-3-thiazoline oxime are dissolved in 100 ml of chloroform. To the solution are added 15 ml (0.252 mol) of freshly distilled methyl isocyanate as well as 3 drops of triethylamine. The mixture, which warms slightly after a short time, is left to stand at room temperature for 16 hours. Subsequently, the slightly turbid solution is filtered, and the solvent and excess methyl isocyanate are distilled off in vacuo. The oily residue is purified chromatographically on 250 g of silica gel using ethyl acetate/n-hexane (1:1) for the elution. The solvent is removed by evaporation, and the resulting residue is recrystallized from methyl chloride/n-hexane/diethyl ether to yield 5-oxo-2,2,4-trimethyl-3-thiazoline O-(methylcarbamoyl)oxime as white crystals, m.p. 90°-92° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04514566
Source datasetuspto-grants-1985_04
ORD IDord-ffc950f160e14f50bd29e479ae916c23
Source noteuspto-grants-1985_04