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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042101Generated: November 1, 2026

Ethyl 2-methylacetoacetate → HCID 87126388, compound

https://huagongshe.com/reaction/1042101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-methylacetoacetateHCID 701—
ReactantPotassium HydroxideHCID 14797—
ReactantSodium NitriteHCID 23668193—
ReactantHCID 66725896HCID 66725896—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
ProductHCID 87126388HCID 8712638883%

Reaction Steps

4-{[6-(Methoxymethyl)pyridin-3-yl]oxy}-2-(tetrahydro-2H-pyran-4-yloxy)aniline (23.4 g) was dissolved in 2N hydrochloric acid (55 mL) and acetonitrile (30 mL), and aqueous solution (70 mL) of sodium nitrite (5.86 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 (10.72 g) and potassium hydroxide (11.2 g) in water (100 mL) and ethanol (100 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 100:0, volume ratio) to give the title compound (26 g, yield 83%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557805B2
Source datasetuspto-grants-2013_10
ORD IDord-fdc7790396744db69e127700c4ed582e
Source noteuspto-grants-2013_10