HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → N-Methyl-1,3-benzothiazol-6-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 18998810 | HCID 18998810 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | N-Methyl-1,3-benzothiazol-6-amine | HCID 10630860 | 19% |
Reaction Steps
To 6-Trifluoroacetamidobenzothiazole (1.97 g, 8 mmol) in 40 ml dry acetone was added methyl iodide (4.54 g, 32 mmol) and then KOH (2.1 g, 32 mmol). The mixture was refluxed for 40 min. and concentrated in vacuo. The product was taken up in 40 ml H2O, refluxed for 40 min. and extracted with methylene chloride. The organic phase was washed with water, dried over Na2SO4 and concentrated in vacuo. The product was purified by flash chromatography (silica gel, methylene chloride) to give 250 mg 6-methylamino-benzothiazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05478845 |
| Source dataset | uspto-grants-1995_12 |
| ORD ID | ord-3cac699a41a841f3ba23cbb621c2d77f |
| Source note | uspto-grants-1995_12 |