HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196451Generated: October 30, 2026
Trifluoromethanesulfonic acid → Distearyl dimethyl ammonium trifluoromethyl sulfonate
https://huagongshe.com/reaction/1196451
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Reactant | Dimethyldioctadecylammonium methyl sulfate | HCID 77450 | — |
| Solvent | Water | HCID 962 | — |
| Product | Distearyl dimethyl ammonium trifluoromethyl sulfonate | HCID 18186058 | — |
Reaction Steps
To 500 milliliters of water was cautiously added 43 milliliters (72.9 grams, 0.486 mol) of trifluoromethane sulfonic acid, CF3SO3H (3M Corporation, Fluorad FC-24, anhydrous). This solution was cooled to room temperature then added to a suspension of distearyl dimethyl ammonium methyl sulfate (DDAMS) (150 grams, 0.227 mol) in 600 milliliters water. The mixture was heated on a hot plate with stirring (80° to 90° C.) for 4 hours, cooled to room temperature and allowed to stand overnight (16 hours). The mixture had separated into a tan solid layer atop the aqueous layer. The solid layer was broken up and the aqueous phase removed by filtration under reduced pressure. The tan solid was washed with water then air dried for 1 hour. The crude material was recrystallized from acetone to afford 114.7 grams (0.164 mol, 72 percent theory), m.p. 90° C. (soften), 119° C. (liquid) of the above trifluoromethane sulfonate salt (DDATRIF), as an off-white powder. A second crop, 17 grams of a tan-yellow solid, was unacceptable for use without further extensive purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05114821 |
|---|
| Source dataset | uspto-grants-1992_05 |
|---|
| ORD ID | ord-f2883ea9c3624f14ab451980f5d52ef5 |
|---|
| Source note | uspto-grants-1992_05 |
|---|