Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64970Generated: October 29, 2026

Potassium Iodide → Diethyl 12H-benzo[a]phenothiazin-5-yl phosphate

https://huagongshe.com/reaction/64970

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
ReactantDiethyl chlorophosphateHCID 13139—
ReactantCarbonate IonHCID 19660—
Reactant5-hydroxy-12H-benzo[a]phenothiazineHCID 13712478—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductDiethyl 12H-benzo[a]phenothiazin-5-yl phosphateHCID 13712499—

Reaction Steps

To a solution of 5-hydroxy-12H-benzo[a]phenothiazine (1.5 g) and diethyl chlorophosphate (2 ml) in DMF (20 ml) there was added a powdered mixture of potassium carbonate (2 g) and potassium iodide (2 g). The reaction mixture was stirred at room temperature. After 30 minutes, a further addition of potassium carbonate and potassium iodide (2 g each) was made and stirring was continued. Two hours later more carbonate (2 g) and diethyl chlorophosphate (2 ml) were added, and then three hours later a final addition of carbonate (2 g) was made. The mixture was stirred for 3 days then diluted with ethyl acetate (60 ml) and the insolubles filtered. The filtrate was washed with water, dried and evaporated down. This residue was crystallized from acetone, then chromatographed on a column of silica gel, eluting first with 1:1, then 3:1 mixtures of ethyl acetate and hexane to afford pure title compound (337 mg), m.p. 162°-163° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04611056
Source datasetuspto-grants-1986_09
ORD IDord-b19ed31449ef4fa6856a3ace05b8b6b6
Source noteuspto-grants-1986_09