Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281879Generated: October 31, 2026

Butyryl chloride → 2-Butyrylthieno[2,3-b][1,5]benzoxazepin-4(5H)-one

https://huagongshe.com/reaction/1281879

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyryl chlorideHCID 8855—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantThieno[2,3-b][1,5]benzoxazepin-4(5H)-oneHCID 18422172—
Solvent1,2-DichloroethaneHCID 11—
Product2-Butyrylthieno[2,3-b][1,5]benzoxazepin-4(5H)-oneHCID 1842231460.5%

Reaction Steps

Thieno[2,3-b][1,5]benzoxazepin-4(5H)-one (1.5 g) was suspended in 1,2-dichloroethane (20 ml) and butyryl chloride (880 mg) was added. To this reaction system was added portionwise aluminium chloride (4.6 g) under ice-cooling. The mixture was stirred at room temperature for 45 minutes. Insoluble matter was filtrated and the filtrate was poured into ice water, and chloroform was added. The organic layer was washed with water and dried over sodium sulfate. The solvent was evaporated under reduced pressure and water-ethanol was added. The precipitated crystals were collected by filtration. The obtained crystals were washed with chloroform-diisopropyl ether to give 2-butyrylthieno[2,3-b][1,5]benzoxazepin-4(5H)-one (1.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06455521B1
Source datasetuspto-grants-2002_09
ORD IDord-b2839bbcf33440e8a15e16467d243ac3
Source noteuspto-grants-2002_09