HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380643Generated: October 30, 2026
Hydrochloric Acid → Ethyl 2-bromo-3-oxobutanoate
https://huagongshe.com/reaction/1380643
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-Hydroxyethyl radical | HCID 119440 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 4H-1,3-Dioxin-4-one, 5-bromo-2,2,6-trimethyl- | HCID 10353435 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Ethyl 2-bromo-3-oxobutanoate | HCID 11206579 | 65.7% |
Reaction Steps
Sodium metal (13.7 g, 0.59 mol) was dissolved in 500 ml of absolute ethanol, and the resulting ethoxide solution was cooled to 0° C. Crude 5-bromo-2,2,6-trimethyl-4H-1,3-dioxin-4-one (115.5 g, 0.5 mole at 95% purity) was then added, dropwise, to the chilled ethoxide solution over 30 minutes and the dark orange reaction mixture was stirred an additional 30 minutes at 0° C. The reaction was poured into 500 ml of ether and 550 ml of 1N HCl, and the organic layer was washed repeatedly with water (4×250 ml) and then dried over Na2SO4. Removal of solvent in vacuo (30° C., 2 Torr), followed by distillation on a 2-inch wiped-film molecular still (120° C. jacket, 0.2 Torr) afforded 68.7 g (71%) of a pale yellow oil (98% pure by gc).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04582913 |
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| Source dataset | uspto-grants-1986_04 |
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| ORD ID | ord-6207dcc131b74f48a3c4aecd640d3da3 |
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| Source note | uspto-grants-1986_04 |
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