Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261673Generated: October 25, 2026

Hydrogen Bromide → Butanoic acid, 4-bromo-2-(methoxyimino)-3-oxo-, ethyl ester

https://huagongshe.com/reaction/261673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantBromineHCID 24408—
ReactantEthyl (2Z)-2-methoxyimino-3-oxo-butanoateHCID 43493—
SolventAcetic AcidHCID 176—
SolventCarbon TetrachlorideHCID 5943—
ProductButanoic acid, 4-bromo-2-(methoxyimino)-3-oxo-, ethyl esterHCID 54053279—

Reaction Steps

Bromine (100 g.) was dropwise added over 40 minutes under reflux to a solution of ethyl 2-methoxyiminoacetoacetate (a mixture of syn and anti isomers) (100 g.) in a mixture of carbon tetrachloride (300 ml.) and acetic acid (300 ml.). The mixture was stirred at 70° to 80° C. until the evolution of hydrogen bromide ceased. The reaction mixture was washed twice with water (300 ml.), a sodium bicarbonate aqueous solution and a saturated sodium chloride aqueous solution and dried over magnesium sulfate. The solution was treated with activated charcoal (2 g.) and concentrated under reduced pressure to give ethyl 2-methoxyimino-4-bromoacetoacetate (a mixture of syn and anti isomers) (120.8 g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04166115
Source datasetuspto-grants-1979_08
ORD IDord-207f3892e14f4f30b0ca214fd23a7b11
Source noteuspto-grants-1979_08