HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 344709Generated: October 26, 2026
Methyl iodide → 5-Chloro-2-(methylthio)benzothiazole
https://huagongshe.com/reaction/344709
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178527796 | HCID 178527796 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Chloro-2-(methylthio)benzothiazole | HCID 645746 | 98.1% |
Reaction Steps
With stirring under ice cooling, 2.00 g (9.92 mmols) of 5-chloro-2-mercaptobenzothiazole was added gradually to 10 ml of a solution of 0.24 g (10.00 mmols) of sodium hydroxide in dimethylformamide (DMF). The mixture was dropwise added to 20 ml of a solution of 0.62 ml (9.96 mmols) of iodomethane in 20 ml of DMF with stirring under ice cooling and the mixture was stirred for further 30 minutes under ice cooling. The mixture was concentrated under reduced pressure, and to the residue was added an aqueous saturated sodium bicarbonate followed by extraction of the solution with chloroform. The chloroform layer was dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: chloroform/methanol =100/1) to afford 2.10 g (yield: 98%) of 5-chloro-2-methylthiobenzothiazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05053408 |
|---|
| Source dataset | uspto-grants-1991_10 |
|---|
| ORD ID | ord-042dce2aab6841d0a8823b8c8bcc9c6c |
|---|
| Source note | uspto-grants-1991_10 |
|---|