HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170218Generated: October 30, 2026
Ethyl Acetoacetate → HCID 90386888, compound
https://huagongshe.com/reaction/2170218
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Bromo-1-(2-phenoxyphenyl)ethan-1-one | HCID 13074046 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 90386888 | HCID 90386888 | 100% |
Reaction Steps
A mixture of sodium hydride (60% oil dispersion, 0.157 g, 3.92 mmol) and tetrahydrofuran (6.1 mL) was cooled to 0° C., treated dropwise with ethyl 3-oxobutanoate (0.413 mL, 3.27 mmol) and stirred at 0° C. for 30 minutes. A solution of 2-bromo-1-(2-phenoxyphenyl)ethanone (1.05 g, 3.6 mmol) in tetrahydrofuran (2 mL) was added dropwise and stirring was continued for 5.5 hours. The reaction mixture was partitioned between ethyl acetate and saturated aqueous ammonium chloride solution and washed with saturated aqueous sodium chloride. The combined aqueous layers were extracted with ethyl acetate. The combined organic layers were dried over anhydrous magnesium sulfate, filtered and concentrated. The residue was purified by flash chromatography (silica gel, 2-20% ethyl acetate in hexanes) to give 1.1 g (100%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09050346B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-b86ab3aef3524b218422c8725519ab11 |
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| Source note | uspto-grants-2015_06 |
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