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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-Hydroxyethyl radicalHCID 119440—
ReactantSodiumHCID 5360545—
Reactant4H-1,3-Dioxin-4-one, 5-bromo-2,2,6-trimethyl-HCID 10353435—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
ProductEthyl 2-bromo-3-oxobutanoateHCID 1120657965.7%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04582913
Source datasetuspto-grants-1986_04
ORD IDord-6207dcc131b74f48a3c4aecd640d3da3
Source noteuspto-grants-1986_04