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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042112Generated: November 3, 2026

Ethyl 2-methylacetoacetate → HCID 87126376, compound

https://huagongshe.com/reaction/1042112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-methylacetoacetateHCID 701—
ReactantPotassium HydroxideHCID 14797—
ReactantSodium NitriteHCID 23668193—
ReactantHCID 66726077HCID 66726077—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
ProductHCID 87126376HCID 8712637659%

Reaction Steps

4-({6-[(2-Methoxyethoxy)methyl]pyridin-3-yl}oxy)-2-(tetrahydro-2H-pyran-4-yloxy)aniline (7.84 g) was dissolved in 2N hydrochloric acid (20 mL) and acetonitrile (15 mL), and aqueous solution (20 mL) of sodium nitrite (1.73 g) was added dropwise under ice-cooling. After the completion of the dropwise addition, the reaction mixture was stirred under ice-cooling for 30 min. The reaction mixture was added dropwise to a solution of ethyl 2-methylacetoacetate (3.17 g) and potassium hydroxide (3.3 g) in water (70 mL) and ethanol (70 mL) at −20° C. After stirring at −20° C. for 30 min, water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over magnesium sulfate, filtered and concentrated under reduced pressure. The obtained crude product was subjected to silica gel column chromatography (ethyl acetate:hexane=0:100 to 85:15, volume ratio) to give the title compound (6.0 g, yield 59%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557805B2
Source datasetuspto-grants-2013_10
ORD IDord-fc74e71f8d3249549e3e5b99c8052f4c
Source noteuspto-grants-2013_10