HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 979092Generated: October 29, 2026
Methyl iodide → 4-Bromo-2,3,7-trimethoxy-10H-phenothiazine
https://huagongshe.com/reaction/979092
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-bromo-2,7-dimethoxy-3-hydroxy-10H-phenothiazine | HCID 13853738 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Bromo-2,3,7-trimethoxy-10H-phenothiazine | HCID 13882038 | 36.7% |
Reaction Steps
To a solution of 4-bromo-2,7-dimethoxy-3-hydroxy-10H-phenothiazine (3.54 g) and methyliodide (2.5 ml) in DMF (20 ml) there was added pulverized potassium carbonate (1.3 g). The reaction mixture was stirred at room temperature. After 15 minutes, another addition of potassium carbonate (1 gram) was made, followed by two other such additions at 15-minute intervals. The final mixture was stirred for a further 15 minutes, then it was diluted with water (100 ml) and ethyl acetate (100 ml). The organic layer was washed twice with water, dried and evaporated down to a solid residue. Crystallization from acetone followed by column chromatography on silica gel eluting with 1:19 ethyl acetate-dichloromethane afforded the pure title compound (1.27 g). m.p. 223°-225° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04666907 |
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| Source dataset | uspto-grants-1987_05 |
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| ORD ID | ord-e805811533434951985b0b30723bfce5 |
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| Source note | uspto-grants-1987_05 |
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