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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231058Generated: November 3, 2026

Methyl iodide → 4-Bromo-2,3,7-trimethoxy-10H-phenothiazine

https://huagongshe.com/reaction/231058

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant4-bromo-2,7-dimethoxy-3-hydroxy-10H-phenothiazineHCID 13853738—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-Bromo-2,3,7-trimethoxy-10H-phenothiazineHCID 1388203836.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04845083
Source datasetuspto-grants-1989_07
ORD IDord-bfe542a4bbf14ecbbad90eae15d95663
Source noteuspto-grants-1989_07