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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Methyl chloroacetate | HCID 7295 | — |
| Reactant | Cyclohexanone | HCID 7967 | — |
| Reactant | Dimethylolpropionic acid | HCID 78501 | — |
| Reactant | Carbonoperoxoic acid | HCID 181880 | — |
| Reactant | Triethylammonium 2,2-bis-(hydroxymethyl)-propionate | HCID 20262776 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Carbomethoxymethyl 2,2-bis-(hydroxymethyl)-propionate | HCID 20442485 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04477642 |
|---|
| Source dataset | uspto-grants-1984_10 |
|---|
| ORD ID | ord-b05d94b324fe497bb77ef6a7d76ce2a2 |
|---|
| Source note | uspto-grants-1984_10 |
|---|