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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128021Generated: October 28, 2026

Acetic Anhydride → HCID 23471553, compound

https://huagongshe.com/reaction/128021

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantHCID 23471568HCID 23471568—
SolventChloroformHCID 6212—
ProductHCID 23471553HCID 2347155346.8%

Reaction Steps

A solution of 13.6 g of 6-(5-hydroxymethyl-3-oxo-2,3,4,5-tetrahydropyridazin-6-yl)-1-methyl-1,2,3,4-tetrahydroquinolin-2-one, 5.8 g of acetic anhydride and 10 ml of triethylamine in 300 ml of chloroform was heated under reflux on a water bath for 3 hours. The reaction mixture was washed with water, dried over potassium carbonate and concentrated under reduced pressure. The residue was dissolved into a small amount of ethyl acetate. After the solution was allowed to stand, the precipitated crystals were filtered off and recrystallized from isopropanol to give 7.3 g of 6-(5-acetoxymethyl-3-oxo-2,3,4,5-tetrahydropyridazin-6-yl)-1-methyl-1,2,3,4-tetrahydroquinolin-2-one as needles, melting at 149°-153° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04258185
Source datasetuspto-grants-1981_03
ORD IDord-2460886106524f7ba1b851a1747efc93
Source noteuspto-grants-1981_03