HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256106Generated: October 31, 2026
Triethylamine → N,N-Diethyl-N-{[3-(trifluoromethyl)phenyl]methyl}ethanaminium chloride
https://huagongshe.com/reaction/256106
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-(Trifluoromethyl)benzyl chloride | HCID 69716 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N,N-Diethyl-N-{[3-(trifluoromethyl)phenyl]methyl}ethanaminium chloride | HCID 13961958 | — |
Reaction Steps
A mixture of 15.3 grams (0.08 mole) of 3-(trifluoromethyl)benzyl chloride and 8.0 grams (0.086 mole) of triethylamine in 50 milliliters of acetonitrile was heated 6 hours at 85° C. The mixture was then stirred over a weekend at room temperature. The crystals which formed were slurried in ethyl ether. The crude product was recovered by filtration and extracted with 600 milliliters of hot methyl ethyl ketone and 0.50 ml of methylene dichloride. The triethyl-(3-trifluoromethyl)benzyl) ammonium chloride was recoved by filtration in a yield of 13.7 grams. The product melted at 213°-215° C. The structure of the compound was confirmed by NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04701211 |
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| Source dataset | uspto-grants-1987_10 |
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| ORD ID | ord-aac5cef9dc2b4b7da5062e3bf09bef96 |
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| Source note | uspto-grants-1987_10 |
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