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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 71695Generated: October 26, 2026

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

https://huagongshe.com/reaction/71695

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 numberUS08822430B2
Source datasetuspto-grants-2014_09
ORD IDord-fca9257d177c4db48fcc022aeba638b3
Source noteuspto-grants-2014_09