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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Diethyl chlorophosphate | HCID 13139 | — |
| Reactant | Carbonate Ion | HCID 19660 | — |
| Reactant | 5-hydroxy-12H-benzo[a]phenothiazine | HCID 13712478 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Diethyl 12H-benzo[a]phenothiazin-5-yl phosphate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04611056 |
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| Source dataset | uspto-grants-1986_09 |
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| ORD ID | ord-b19ed31449ef4fa6856a3ace05b8b6b6 |
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| Source note | uspto-grants-1986_09 |
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