HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl p-toluenesulfonate → Benzothiazolium, 3-methyl-2-(methylthio)-, 4-methylbenzenesulfonate (1:1)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl p-toluenesulfonate | HCID 6645 | — |
| Reactant | 2-(Methylthio)-6-nitro-1,3-benzothiazole | HCID 305552 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Benzothiazolium, 3-methyl-2-(methylthio)-, 4-methylbenzenesulfonate (1:1) | HCID 41464 | 63.6% |
Reaction Steps
A mixture of 6-nitro-2-(methylthio)benzothiazole 7 (0.5 g, 2.2 mmol) and methyl-p-toluenesulfonate (3.7 g, 20 mmol) was heated from 120° C. to 145° C. over one hour. To the cooled solution was added 30 mL of ether. The resulting amorphous solid was triturated with acetone to provide a pale mauve solid (0.57 g, 1.4 mmol, 63%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06541618B1 |
| Source dataset | uspto-grants-2003_04 |
| ORD ID | ord-86c70a75294545d29a0310333ff14a33 |
| Source note | uspto-grants-2003_04 |