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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440162Generated: October 25, 2026

Ethyl 3,3-dimethylacrylate → Ethyl-4-bromo-3-methyl-but-2-enoate (E/Z; 55/45)

https://huagongshe.com/reaction/440162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3,3-dimethylacrylateHCID 12516—
ReactantN-bromobutanimideHCID 67184—
CatalystAzobisisobutyronitrileHCID 6547—
SolventCarbon TetrachlorideHCID 5943—
ProductEthyl-4-bromo-3-methyl-but-2-enoate (E/Z; 55/45)HCID 53411540106.5%

Reaction Steps

The olefins 66 can also be prepared by reacting the corresponding substituted phenols with ethyl 4-bromo-3-methyl-2-butenate in the presence of potassium carbonate and small amount of 18-crown-ether in methylene chloride. The starting material ethyl 4-bromo-3-methylbutenate has been obtained from the reaction of ethyl 3,3-dimethylacrylate with N-bromosuccinimide (NBS) as follows: to 20 g of ethyl 3,3-dimethylacrylate in 250 ml of carbon tetrachloride, 30 g of N-bromosuccinimide (NBS) and 0.01 g of azobisisobutyronitrile were added. The mixture was refluxed for 3 hours. Succinimide was removed by filtration and the filtrate was washed with chloroform. The combined organic layers were washed sequentially with saturated sodium sulfite, saturated sodium chloride and then dried over anhydrous magnesium sulfate. Evaporation of the solvent afforded 34.4 g ethyl 4-bromo-3-methyl-2-butenate (Safaryn, J. E.; Chiarello, J.; Chen, K. M.; Joullie, M. M.; Tetrahedron, 1986, 42, 2635). The product can be further purified by silica gel flash column chromatography using ether/hexane (e.g. 1:50) as eluent, and hydrolyzed to the corresponding carboxylic acid with aqueous methanolic NaOH. ##STR12## wherein R1 =H, CF3, R or OR;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05516931
Source datasetuspto-grants-1996_05
ORD IDord-ed4dcd43841c43f48de476e6875c7051
Source noteuspto-grants-1996_05