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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1947710Generated: October 30, 2026

Lithium Hydroxide → [4-Methyl-6-oxopyridazin-1(6H)-yl]acetic acid

https://huagongshe.com/reaction/1947710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HydroxideHCID 3939—
ReactantTrifluoroacetic acidHCID 6422—
Reactantethyl [4-methyl-6-oxopyridazin-1(6H)-yl]acetateHCID 77231410—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product[4-Methyl-6-oxopyridazin-1(6H)-yl]acetic acidHCID 66939440—

Reaction Steps

To ethyl [4-methyl-6-oxopyridazin-1(6H)-yl]acetate (0.575 g, 2.93 mmol) in tetrahydrofuran (3 mL), methanol (2 mL) and water (2 mL) was added 1 N lithium hydroxide solution (2.9 mL). The reaction mixture was stirred at ambient temperature for 1.5 h. After neutralized with trifluoro acetic acid, the reaction mixture was directly purified by reverse phase HPLC (TMC Pro-Pac C18; 0-45% 0.1% trifluoroacetic acid in acetonitrile/0.1% trifluoroacetic acid in water gradient). The pure fractions were lyophilized overnight to yield the title compound. LC/MS 169.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399480B2
Source datasetuspto-grants-2013_03
ORD IDord-f74fef564e6d4da583fd4e4cc8340286
Source noteuspto-grants-2013_03