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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650009Generated: October 31, 2026

Hydrochloric Acid → 2-isopropenylthieno[2,3-b][1,5]benzoxazepin-4(5H)-one

https://huagongshe.com/reaction/650009

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-acetylthieno[2,3-b][1,5]benzoxazepin-4(5H)-oneHCID 18422337—
ReactantHCID 86584867HCID 86584867—
SolventDiethyl EtherHCID 3283—
Product2-isopropenylthieno[2,3-b][1,5]benzoxazepin-4(5H)-oneHCID 18422274—

Reaction Steps

2-Acetylthieno[2,3-b][1,5]benzoxazepin-4(5H)-one (1.8 g) was suspended in ether (15 ml) and 20 equivalent amounts of magnesium methyl iodide was added under ice-cooling. The mixture was stirred at room temperature for 24 hours. The reaction mixture was poured into 1M hydrochloric acid under ice-cooling and insoluble matter was filtered off. The resulting mixture was extracted twice with chloroform. The chloroform layer was dried over sodium sulfate and the solvent was evaporated under reduced pressure. The residue was suspended in toluene and a catalytic amount of p-toluenesulfonic acid was added. The mixture was stirred under reflux with heating for 20 minutes. The reaction system was cooled to room temperature and the reaction mixture was washed with saturated aqueous sodium hydrogencarbonate solution. The solvent was evaporated under reduced pressure and diisopropyl ether was added to the residue. The precipitated crystals were collected by filtration to give 2-isopropenylthieno[2,3-b][1,5]benzoxazepin-4(5H)-one (800 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06271225B1
Source datasetuspto-grants-2001_08
ORD IDord-61d4620c77cf439b80f233876d6d4ccd
Source noteuspto-grants-2001_08