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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477183Generated: October 30, 2026

Acetic Anhydride → HCID 56609064, compound

https://huagongshe.com/reaction/477183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 73474322HCID 73474322—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 56609064HCID 56609064—

Reaction Steps

5.3 Grams of 6-[4-(2-phenyl-2-hydroxyiminoethyl)-1-piperazinylcarbonyl]-3,4-dihydrocarbostyril, 1.91 ml of acetic anhydride and 5.64 ml of triethylamine were dissolved in 60 ml of methylene chloride, and the resulting solution was stirred overnight at room temperature. After the reaction was completed, the reaction mixture was poured into water, and was made alkaline by adding sodium carbonate, then this mixture was extracted with methylene chloride. The methylene chloride extract was dried, then the solvent was removed by evaporation, and the residue was converted into an oxalate by stirring with oxalic acid in acetone. The oxalate was recrystallized from ethanol-water to yield 5.28 g of 6-[4-(2-phenyl-2-acetoxyiminoethyl)-1-piperazinylcarbonyl]-3,4-dihydrocarbostyril.oxalate.monohydrate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04886809
Source datasetuspto-grants-1989_12
ORD IDord-2d9dbc8d535540ffbdda65b1b8a4e30c
Source noteuspto-grants-1989_12