HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383110Generated: October 26, 2026
Ethyl Acetoacetate → Ethyl 4-bromo-3-oxobutanoate
https://huagongshe.com/reaction/383110
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Reactant | Bromine | HCID 24408 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Ethyl 4-bromo-3-oxobutanoate | HCID 575284 | 73.9% |
Reaction Steps
To a mechanically-stirred solution of ethyl acetoacetate (59 mL, 463 mmol) in ether (75 mL) was added bromine (23.5 mL, 912 mmol) while the reaction temperature was maintained below 23° C. using an ice-water bath. The yellow-orange solution was stirred for 5 hours with cooling and then was stirred overnight at ambient temperature. Ice (60 g) was added and the reaction mixture was extracted with ether. The organic phase was washed twice with aqueous NaHCO3 saturated with NaCl and once with brine. The ether solution was stirred for 1 day over CaCl2 and then was filtered through celite. The filter cake was rinsed with dichloromethane. The filtrate was concentrated in vacuo to give ethyl 4-bromoacetoacetate (71.5 g) which was stored in the dark and stabilized with BaCO3 (300 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06310095B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-bae8b4558d644111a0b53a1d516e9ec9 |
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| Source note | uspto-grants-2001_10 |
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