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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174325Generated: November 1, 2026

Triethylsilane → 4-Bromo-1-chloro-2-(4-ethoxy-benzyl)-benzene

https://huagongshe.com/reaction/2174325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylsilaneHCID 12052—
ReactantTrifluoromethanesulfonic acidHCID 62406—
Reactant(5-Bromo-2-chlorophenyl)(4-ethoxyphenyl)methanoneHCID 10020105—
SolventTrifluoroacetic acidHCID 6422—
Product4-Bromo-1-chloro-2-(4-ethoxy-benzyl)-benzeneHCID 999644994.4%

Reaction Steps

To (5-bromo-2-chlorophenyl)(4-ethoxyphenyl)methanone (1440 g, 4.26 mol) and triethylsilane (1.37 L, 8.6 mol) in trifluoroacetic acid (820 mL) was slowly added trifluoromethanesulfonic acid (1.9 mL). After refluxing for 6 hours, additional triethylsilane (400 mL, 2.47 mol) was added. After refluxing for another 8 hours, the mixture was evaporated under reduced pressure. The residue was dissolved in dichloromethane (20 L), washed with water (10 L), aqueous sodium carbonate (10 L), and brine (10 L), and concentrated to give crude product. The crude product was distilled to remove (Et3Si)2O under vacuum. The residue was recrystallized from absolute ethanol (5 L) and dried under vacuum to give compound 3 (1310 g, 94% yield, HPLC purity>99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09061060B2
Source datasetuspto-grants-2015_06
ORD IDord-e231fa2d300b41a2b9f45406e73474d0
Source noteuspto-grants-2015_06