HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-Ethyl-2-(4,6-bis-trichloromethyl-s-triazin-2-yl-methylene)benzothiazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,3,5-Triazine, 2,4,6-tris(trichloromethyl)- | HCID 23038 | — |
| Reactant | Benzothiazolium, 3-ethyl-2-methyl-, 4-methylbenzenesulfonate (1:1) | HCID 84711 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-Ethyl-2-(4,6-bis-trichloromethyl-s-triazin-2-yl-methylene)benzothiazoline | HCID 57199265 | — |
Reaction Steps
Within a period of half an hour, 10 g (0.1 mol) of triethylamine was added dropwise to a suspension of 35 g (0.1 mol) of 3-ethyl-2-methyl-benzothiazolium-p-toluene-sulfonate and 43 g (0.1 mol) of tris-trichloromethyl-s-triazine in 300 ml of toluene. After completion of the addition the reaction mixture was stirred for half an hour, until the exothermic reaction ceased; the product which had precipitated was filtered off and dried. Compound 2 was obtained in nearly pure form in a quantity of 40 g. By evaporating the toluene in vacuo and treating the solid residue with ethanol, another 9 g of the product resulted. After recrystallization from 2-methoxy-ethanol 40 g (82%) of yellow needles of melting point 238° to 241° C. were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05212307 |
| Source dataset | uspto-grants-1993_05 |
| ORD ID | ord-5ef6a5ddbfb549e1b1f3c4cd967f388b |
| Source note | uspto-grants-1993_05 |