HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1065973Generated: November 1, 2026
Hydrochloric Acid → Dimethylanilinium chloride
https://huagongshe.com/reaction/1065973
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | HCID 178505971 | HCID 178505971 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Dimethylanilinium chloride | HCID 11789467 | — |
Reaction Steps
Boron trifluoride diethyl etherate (138.7 g, 0.98 mole) is added to a diethyl ether solution of pentafluorophenylmagnesium bromide (3326 g, 4.17 moles) formed as in Example 24. The addition is at a rate allowing the mixture to reach reflux temperature. The mixture is heated at reflux for 18 hours. This mixture is then cooled to −10° C. and N,N-dimethylanilinium chloride (1142 grams, 2.06 moles) previously formed from concentrated HCl, water, and N,N-dimethylaniline is slowly added while keeping the temperature at about 0° C. After the addition, the mixture is stirred for one hour at −5° C. to 0° C. Then the two phases are separated, and the organic phase is washed with water and dried over MgSO4. The N,N-dimethylanilinium tetrakis(pentafluorophenyl)borane is precipitated by addition of hexane with stirring, and recovered by filtration.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06241917B1 |
|---|
| Source dataset | uspto-grants-2001_06 |
|---|
| ORD ID | ord-3261a0b85e884198af6906903d3622ae |
|---|
| Source note | uspto-grants-2001_06 |
|---|