HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042112Generated: November 3, 2026
Ethyl 2-methylacetoacetate → HCID 87126376, compound
https://huagongshe.com/reaction/1042112
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 2-methylacetoacetate | HCID 701 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | HCID 66726077 | HCID 66726077 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 87126376 | HCID 87126376 | 59% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08557805B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-fc74e71f8d3249549e3e5b99c8052f4c |
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| Source note | uspto-grants-2013_10 |
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