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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198775Generated: October 31, 2026

Phosgene → HCID 15766843, compound

https://huagongshe.com/reaction/1198775

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
ReactantDiphosgeneHCID 10426—
ReactantSodium HydroxideHCID 14798—
Reactant2-Chloro-4-fluorophenolHCID 74814—
CatalystMethaneHCID 297—
SolventDichloromethaneHCID 6344—
ProductHCID 15766843HCID 15766843100%

Reaction Steps

2-Chloro-4-fluorophenol (733 g, 5.0 mol) and methylene chloride (2.5 liters) were put in a 5-liter three-neck flask as equipped with a stirrer, and 4 N sodium hydroxide aqueous solution (1350 ml) was added thereto and stirred with cooling. To the resulting solution was introduced phosgene as generated by decomposing trichloromethyl chloroformate (148 ml, 243 g, 1.23 mol) on an active charcoal (3.8 g) at a temperature of 40° to 50° C. After introduction of phosgene, the reaction solution was further stirred overnight at room temperature. After the reaction, the organic layer was separated, and the aqueous layer was extracted with methylene chloride (500 ml ×2). The organic layers were combined, washed with 1 N sodium hydroxide aqueous solution (1000 ml) and water, and thereafter dried with anhydrous magnesium sulfate. The drying agent was removed, and the solvent was removed by distillation under reduced pressure to obtain a white solid of bis (2-chloro-4-fluorophenyl)carbonate (801g 5.0 mol). Yield: 100 %. m.p.: 91.0° to 92.0° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05281742
Source datasetuspto-grants-1994_01
ORD IDord-865cd7d134b54cdaa53fcd1ad8a537dc
Source noteuspto-grants-1994_01