HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trichloroacetyl chloride → 2-Trichloroacetylmethylene-3-ethyl-benzothiazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trichloroacetyl chloride | HCID 6420 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzothiazolium, 3-ethyl-2-methyl-, 4-methylbenzenesulfonate (1:1) | HCID 84711 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Trichloroacetylmethylene-3-ethyl-benzothiazoline | HCID 54396017 | — |
Reaction Steps
10 g (28.6 mmol) of 2-methyl-3-ethyl-benzothiazolium p-toluenesulfonate are suspended in 150 ml of toluene, 6.8 g (67.2 mmol) of triethylamine are added and, at 5°-10° C. 6 g (33 mmol) of trichloroacetyl chloride, dissolved in a minor amount of toluene, are added dropwise. After three hours at room temperature, the ammonium salts are filtered off with suction, and the reaction solution is washed with water, dried over sodium sulfate and concentrated in vacuo. The product is caused to crystallize from the diisopropyl ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04966828 |
| Source dataset | uspto-grants-1990_10 |
| ORD ID | ord-d6002d5007a34608ac0debe48ba35e09 |
| Source note | uspto-grants-1990_10 |