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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632797Generated: November 2, 2026

Potassium Iodide → Carbomethoxymethyl 2,2-bis-(hydroxymethyl)-propionate

https://huagongshe.com/reaction/1632797

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantMethyl chloroacetateHCID 7295—
ReactantCyclohexanoneHCID 7967—
ReactantDimethylolpropionic acidHCID 78501—
ReactantCarbonoperoxoic acidHCID 181880—
ReactantTriethylammonium 2,2-bis-(hydroxymethyl)-propionateHCID 20262776—
SolventTriethylamineHCID 8471—
ProductCarbomethoxymethyl 2,2-bis-(hydroxymethyl)-propionateHCID 20442485—

Reaction Conditions

Temperature100 °C

Reaction Steps

A 5-liter reaction vessel which has been equipped with a stirrer, an internal thermometer, a reflux condenser and a 1-liter dropping funnel is charged with 550 g of 2,2-bis-(hydroxymethyl)-propionic acid and 2,460 g of cyclohexanone, and the mixture is heated to 100° C. When the bulk of the dihydroxycarboxylic acid has gone into solution, the temperature is lowered to 60° C., and 414 g of triethylamine are added dropwise. The temperature is held at 60° C. by cooling. The resulting triethylammonium 2,2-bis-(hydroxymethyl)-propionate stays in solution. 7 g of potassium iodide are then added, followed, in dropwise fashion, by 565 g of methyl chloroacetate in the course of 30 minutes. The batch is held at this temperature for a further 4 hours, is then allowed to cool down to room temperature and is filtered to remove the triethylammonium chloride formed. The filtrate is concentrated in a rotary evaporator and is then adjusted with xylene to a solids content of 90%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04477642
Source datasetuspto-grants-1984_10
ORD IDord-b05d94b324fe497bb77ef6a7d76ce2a2
Source noteuspto-grants-1984_10