Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21910218 | HCID 21910218 | 70% |
Reaction Steps
19.07 g (0.1 mol) of tosyl chloride, 12.12 g (0.1 mol) of N,N-dimethylaniline and 10.1 g (0.1 mol) of triethylamine were dissolved in 60 g of tetrahydrofuran, and, after cooling to 10° C., there was added 10.81 g (0.1 mol) of benzyl alcohol. While suppressing excessive elevation of the temperature, the reaction was allowed for 5 hours. After the completion of the reaction, the mixture was concentrated, and the precipitated white solid was washed with ether and dried to give N-benzyl-N,N-dimethylanilinium tosylate. Yield: 70%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05349067 |
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| Source dataset | uspto-grants-1994_09 |
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| ORD ID | ord-807ef9d8256d4330b7ae5466c7f98255 |
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| Source note | uspto-grants-1994_09 |
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