HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226637Generated: November 1, 2026
4-Toluenesulfonyl chloride → HCID 15218866, compound
https://huagongshe.com/reaction/2226637
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Dicyclohexylamine | HCID 7582 | — |
| Reactant | 4-Methoxybenzyl alcohol | HCID 7738 | — |
| Reactant | N-Ethyl-N-methylaniline | HCID 11956 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 15218866 | HCID 15218866 | 50% |
Reaction Steps
19.07 g (0.1 mol) of tosyl chloride, 13.5 g (0.1 mol) of N-ethyl-N-methylaniline and 27.20 g (0.15 mol) of dicyclohexylamine were dissolved in 60 g of dichloromethane, and, after cooling to 5° C., there was added 13.81 g (0.1 mol) of 4-methoxybenzylalcohol. While suppressing excessive elevation of the temperature, the reaction was allowed for 6 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-(4-methoxybenzyl)-N-ethyl-N-methyl-anilinium tosylate. Yield: 50%.
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-9f9365111fb946fc9f86c79e2a54176b |
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| Source note | uspto-grants-1994_09 |
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