HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → 2-[4-(4,6-Bis-trichloromethyl-s-triazin-2-yl) benzoylmethylene]-3-methylbenzothiazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | HCID 14473251 | HCID 14473251 | — |
| Reactant | 2,3-Dimethyl-benzothiazolium p-toluenesulfonate | HCID 86745136 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 2-[4-(4,6-Bis-trichloromethyl-s-triazin-2-yl) benzoylmethylene]-3-methylbenzothiazoline | HCID 86745137 | — |
Reaction Steps
2,3-Dimethylbenzothiazolium-p-toluenesulfonate (13.4 pbw) and 4-(4,6-bis-trichloromethyl-s-triazin2-yl)-benzoylchloride (22.7 pbw) are successively suspended or dissolved, respectively, in 150 pbw of toluene. The mixture is cooled to 15° C. and with the exclusion of moisture 13.1 pbw of triethylamine are added dropwise at this temperature. The mixture discolors towards dark brown and is stirred for 3 hours at room temperature. The precipitate formed is removed by filtration with suction and washed with cold toluene. The residue is digested in 200 pbw of methanol and stirred for about 60 minutes, again filtered and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05055579 |
| Source dataset | uspto-grants-1991_10 |
| ORD ID | ord-c979926e303f4c88b1dbb09f16ae3759 |
| Source note | uspto-grants-1991_10 |