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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 394440Generated: October 26, 2026

Diphosgene → 3-(4-Chloro-6-fluoro-2-methoxy-3-nitrophenyl)-1,5-dimethyl-6-thioxo-[1,3,5]triazinane-2,4-dione

https://huagongshe.com/reaction/394440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiphosgeneHCID 10426—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantN,N'-DimethylthioureaHCID 2723631—
Reactant4-Chloro-6-fluoro-2-methoxy-3-nitrophenylamineHCID 18176019—
SolventTolueneHCID 1140—
SolventTriethylamineHCID 8471—
Product3-(4-Chloro-6-fluoro-2-methoxy-3-nitrophenyl)-1,5-dimethyl-6-thioxo-[1,3,5]triazinane-2,4-dioneHCID 18176008—

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 3.0 g (15.0 mmol) of diphosgene in 5 ml of toluene was added dropwise at approximately 20° C. to a solution of 3.0 g (13.6 mmol) of 4-chloro-6-fluoro-2-methoxy-3-nitrophenylamine in 15 ml of toluene. Then, the mixture was slowly heated to reflux temperature and stirred for 6 hours under reflux. After the reaction mixture had been concentrated and dried, the crude isocyanate was redissolved in 5 ml of toluene to be used in the next reaction. 6 ml of triethylamine and a solution of 3.55 g (14.4 mmol) of dimethylthiourea were added dropwise to this solution at approximately 20° C. 4.7 g (28.8 mmol) of carbonyldiimidazole were subsequently added to the reaction mixture. The mixture was heated at 80° C. for 5 hours and then allowed to cool. For work-up, it was firstly washed four times with water. Then, the organic phase was dried over magnesium sulfate and concentrated under reduced pressure. The crude product (6.58 g) was purified by silica gel chromatography (mobile phase: cyclohexane/ethyl acetate=10:1). Yield: 1.31 g (24%);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06602825B1
Source datasetuspto-grants-2003_08
ORD IDord-ac4b319ced2046b99950b95e610109ee
Source noteuspto-grants-2003_08