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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 979301Generated: October 30, 2026

Methyl iodide → HCID 13853737, compound

https://huagongshe.com/reaction/979301

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 135626448HCID 135626448—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 13853737HCID 1385373780.2%

Reaction Steps

Potassium tert.-butoxide (500 mg) was added to a suspension of 1-hydroxy-6-methyl-5H-benzo[a]phenothiazin-5-one (from Example 32) (500 mg) and methyl iodide (2 ml) in DMF (20 ml). After 30 minutes at room temperature, EtOAc (250 ml) was added followed by water (200 ml). The aqueous layer was decanted and the organic layer was dried and evaporated to dryness. The residue was treated with ether, filtered and air-dried to afford the desired product (420 mg), m.p. 170°-171° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04667032
Source datasetuspto-grants-1987_05
ORD IDord-2da608feb8fc4a22a113e9f1b9e1060e
Source noteuspto-grants-1987_05