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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 67113Generated: October 28, 2026

Bromine → Ethyl 1-(2-acetoxyethyl)-4-bromopyrrole-2-glyoxalate

https://huagongshe.com/reaction/67113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantEthyl 1-(2-acetoxyethyl)pyrrole-2-glyoxalateHCID 12795013—
ReactantEthyl acetate hexaneHCID 21226206—
SolventDichloromethaneHCID 6344—
ProductEthyl 1-(2-acetoxyethyl)-4-bromopyrrole-2-glyoxalateHCID 1279502856.3%

Reaction Conditions

Temperature-75 °C

Reaction Steps

Three ml (58.3 mmole) of bromine is added in a dropwise manner to a stirred solution of 14.77 g (58.3 mmole) of ethyl 1-(2-acetoxyethyl)pyrrole-2-glyoxalate in 200 ml anhydrous dichloromethane, cooled to -75° C. After the addition, the reaction is left at -75° C. for 2.5 hours and then the temperature is allowed to increase to room temperature. The solvent is removed in vacuo, dichloromethane is added to the residue and the solution is washed successively with water, 10% sodium bicarbonate solution and water. The organic phase is dried over sodium sulfate, and the solvent is removed in vacuo. The crude product thus obtained (18.3 g) is subjected to column chromatography on Florisil (1 Kg) using hexane-ethyl acetate (9:1) as the eluting solvent. There is thus obtained upon removal of the solvent, 10.9 g (56%) of ethyl 1-(2-acetoxyethyl)-4-bromopyrrole-2-glyoxalate as an oil having the following physical constants:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04344943
Source datasetuspto-grants-1982_08
ORD IDord-00fdc22f138741beb6add2da08e5184d
Source noteuspto-grants-1982_08