HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503230Generated: October 30, 2026
Ethyl Acetate → Ethyl 2-(3,4-dichlorobenzyl)-3-oxobutanoate
https://huagongshe.com/reaction/1503230
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-(Bromomethyl)-1,2-dichlorobenzene | HCID 639726 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 2-(3,4-dichlorobenzyl)-3-oxobutanoate | HCID 67402529 | — |
Reaction Steps
To a solution of ethyl acetoacetate (1.0 g) in tetrahydrofuran (20 mL) was added sodium hydride (about 60% oil suspension) (0.37 g) in several portions under ice-cooling under a nitrogen atmosphere. After stirring at room temperature for 1 hr, 3,4-dichlorobenzylbromide (1.4 mL) was added to the reaction mixture. After stirring at room temperature for 2 hr, the reaction mixture was poured into a mixture of ethyl acetate and water. The organic phase was washed successively with water and brine, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by column chromatography on silica gel by eluting with toluene. An eluted fraction containing the desired product was recovered and evaporated under reduced pressure to give ethyl 2-acetyl-3-(3,4-dichlorophenyl)propanoate (35) (1.6 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09212169B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-95f5cc8ad77446eda9277125689b4636 |
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| Source note | uspto-grants-2015_12 |
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