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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418302Generated: November 1, 2026

Chloroacetone → HCID 131721167, compound

https://huagongshe.com/reaction/1418302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetoneHCID 6571—
ReactantPotassium CarbonateHCID 11430—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 15390589HCID 15390589—
SolventAcetonitrileHCID 6342—
ProductHCID 131721167HCID 13172116770.9%

Reaction Steps

An acetonitrile (10 mL) solution of 2-(4-chloro-2-fluoro-5-hydroxyphenyl)-5,6-dihydroimidazo [1,5-a] pyridine-1,3[2H, 7H]-dione (0.59 g, 2.0 mmol), potassium carbonate (0.2 g, 2.2 mmol) and chloroacetone (0.18 mL, 2.2 mmol) was stirred for 5 hours under reflux. A saturated ammonium chloride solution (10 mL) was added to the resulting mixture, and the organic layer was separated and then the aqueous layer was extracted with diethyl ether (10 mL×2 times). The organic layer combined was washed with a saturated sodium chloride solution (20 mL) and dried over anhydrous magnesium sulfate. After removal of magnesium sulfate by filtration, the filtrate was evaporated to give crude product, which was purified by silica gel column (Wakogel C-200, ethyl acetate/hexane =1/2) to obtain a white solid of 2-(5-acetonyloxy-4-chloro-2-fluorophenyl)-5,6-dihydroimidazo [l,5-a] pyridine-1, 3[2H, 7H]-dione (0.50 g, yield:70.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05883049
Source datasetuspto-grants-1999_03
ORD IDord-1f7739d30ddd42f192659dce37d71b76
Source noteuspto-grants-1999_03