HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1089402Generated: October 27, 2026
Ethyl p-methylbenzenesulfonate → Benzothiazolium, 3-ethyl-2-methyl-, 4-methylbenzenesulfonate (1:1)
https://huagongshe.com/reaction/1089402
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl p-methylbenzenesulfonate | HCID 6638 | — |
| Reactant | 2-Methylbenzothiazole | HCID 8446 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Benzothiazolium, 3-ethyl-2-methyl-, 4-methylbenzenesulfonate (1:1) | HCID 84711 | — |
Reaction Steps
300 g (2 mol) of 2-methylbenzothiazole and 440 g (2.2 mol) of ethyl p-toluenesulfonate (or a mixture of ethyl o- and p-toluenesulfonate) are heated with stirring to 150° C., the temperature rising to about 200° C. due to the exothermic reaction. After 10 minutes, the mixture is poured into two liters of acetone, and the product which has precipitated is filtered off with suction, washed with acetone and dried in vacuo. Yield 730 g (98%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04966828 |
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| Source dataset | uspto-grants-1990_10 |
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| ORD ID | ord-89a1d61946f14c56b89599dd1f2e90c8 |
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| Source note | uspto-grants-1990_10 |
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