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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2038474Generated: October 30, 2026

Triethylsilane → 4-Bromo-2-(4-(bromomethyl)benzyl)-1-chlorobenzene

https://huagongshe.com/reaction/2038474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylsilaneHCID 12052—
ReactantTrifluoromethanesulfonic acidHCID 62406—
ReactantHCID 59557730HCID 59557730—
SolventTrifluoroacetic acidHCID 6422—
Product4-Bromo-2-(4-(bromomethyl)benzyl)-1-chlorobenzeneHCID 59557743—

Reaction Steps

To a stirred solution of Et3SiH (17 mL) and (5-bromo-2-chlorophenyl)(4-(bromomethyl)phenyl)methanone (intermediate AH) (20.75 g, 54 mmol) in TFA (100 mL) at 30° C. was added CF3SO3H (0.05 mL). Within a few minutes the temperature of the solution increased causing it to reflux violently. After 3 h, the volatiles were removed under reduced pressure. The residue was poured into brine and extracted 3× with ethyl acetate. The combined organic layers were washed 3× with H2O, 2× with aqueous Na2SO4 and 2× with brine, and dried over Na2SO4. The solvent was evaporated under reduced pressure, and the product was purified by column chromatography to obtain pure intermediate AI (15.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575321B2
Source datasetuspto-grants-2013_11
ORD IDord-e78a4695e8e84c4ebc61683d10154646
Source noteuspto-grants-2013_11