Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1185622Generated: October 25, 2026

Water → 2-Bromo-5-(2-bromo-acetyl)-benzoic acid methyl ester

https://huagongshe.com/reaction/1185622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-bromobutanimideHCID 67184—
Reactant(Z)-1-Ethoxy-2-(tributylstannyl)etheneHCID 2763294—
ReactantMethyl 2-bromo-5-iodobenzoateHCID 50998202—
CatalystHCID 178418476HCID 178418476—
Solvent1,4-DioxaneHCID 31275—
Product2-Bromo-5-(2-bromo-acetyl)-benzoic acid methyl esterHCID 5961137781.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

To the solution of 2-bromo-5-iodo-benzoic acid methyl ester (4.33 g, 12.7 mmol) and tributyl(ethoxyvinyl)stannane (4.79 g, 13.3 mmol) in dioxane (56 ml) was added PdCl2(PPh3)2 (322 mg). The mixture was heated at 80° C. for 17 hours and was cooled to 0° C. Water (19 ml) was added, followed by slow addition of NBS (2.33 g, 12.9 mmol) over 10 minutes period. The mixture was stirred at 0° C. for additional 40 minutes, and the solvent was removed under reduced pressure. The mixture was diluted with EtOAc, and was washed with water and brine and dried with sodium sulfate. Concentration and purification by flash column chromatography (hexane/EtOAc=2/1) gave 2-bromo-5-(2-bromo-acetyl)-benzoic acid methyl ester (3.48 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08669234B2
Source datasetuspto-grants-2014_03
ORD IDord-463291f560964626a175027b3b6051fe
Source noteuspto-grants-2014_03