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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582563Generated: November 1, 2026

Phosgene → HCID 86759448, compound

https://huagongshe.com/reaction/1582563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
ReactantMethyl (2,6-dimethylphenyl)carbamateHCID 30212—
ReactantSodium MethoxideHCID 10942334—
CatalystBiphenylHCID 7095—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
ProductHCID 86759448HCID 8675944864.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of toluene (150 mL), biphenyl (0.2 g) and sodium methoxide in methanol (23.76 g, 0.11 mol, 25% by weight) was heated at reflux, and the methanol-toluene azeotrope was removed. The mixture was allowed to cool to 80° C., and toluene (80 mL) was added. To the resulting mixture was added in five portions methyl (2,6-dimethylphenyl)carbamate (17.9 g, 0.1 mol). The methanol formed in the reaction was removed as the above azeotrope. When most of the methanol had been removed, ethylene glycol dimethyl ether (8 mL) was added, and the mixture was distilled until the head temperature reached 110° C. The mixture was allowed to cool to 25° C., and ethylene glycol dimethyl ether (3 mL) was added. The mixture was then added to phosgene in toluene (22.5 g, 0.56 mol, 25% by weight). When the addition was complete, excess phosgene was removed by distillation. The mixture was allowed to cool to 25° C., and then washed with sodium bicarbonate solution (40 mL, saturated). The organic layer was dried and the volatiles removed by evaporation to give 17.21 g (64.5%) of the title compound as a solid. An analytical sample was prepared by column chromatography on silica gel using 1:3 ethyl acetate-hexanes as the eluent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06737383B1
Source datasetuspto-grants-2004_05
ORD IDord-87931d178e4a4d958ad0d3a4c6483f36
Source noteuspto-grants-2004_05