Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1439534Generated: October 26, 2026

Tetrachlorobisphenol A → 2-(3,5-Dichloro-4-hydroxyphenyl)-2-(3,5-dichloro-4-cyanatophenyl)-propane

https://huagongshe.com/reaction/1439534

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrachlorobisphenol AHCID 6619—
ReactantSodium CarbonateHCID 10340—
ReactantCyanogen ChlorideHCID 10477—
ReactantSodium HydroxideHCID 14798—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2-(3,5-Dichloro-4-hydroxyphenyl)-2-(3,5-dichloro-4-cyanatophenyl)-propaneHCID 2139585999.7%

Reaction Steps

36.6 g (0.1 mol) of 2,2-bis-(3,5-dichloro-4-hydroxyphenyl)-propane are suspended in 500 ml of water and 400 ml of methylene chloride. After cooling to about 0° to 3° C, 20 ml (0.4 mol) of cyanogen chloride are added. A solution of 10.6 g of Na2CO3 in 50 ml of water is added dropwise over the course of 90 minutes, with vigorous stirring, in such a way that the pH value of the reaction mixture is constantly kept in the range between 7.5 and 8.5. Thereafter, 1 N NaOH is added in such a way that a pH value of the reaction mixture of about 8.0 is maintained, and persists as the final value. Thereafter, the organic phase is separated off, washed with 100 ml of water and concentrated at room temperature. 39 g (99% of theory) of 2-(3,5-dichloro-4-hydroxyphenyl)-2-(3,5-dichloro-4-cyanatophenyl)-propane are obtained as the residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04060541
Source datasetuspto-grants-1977_11
ORD IDord-13f3c81c6ca146db9978f7c0560d11dd
Source noteuspto-grants-1977_11