Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 920528Generated: October 26, 2026

Trimethylsilyl triflate → 1-[4-(Benzyloxy)-3-methylphenyl]-2-bromoethanone

https://huagongshe.com/reaction/920528

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl triflateHCID 65367—
ReactantN-bromobutanimideHCID 67184—
ReactantDiisopropylethylamineHCID 81531—
ReactantEthanone, 1-[3-methyl-4-(phenylmethoxy)phenyl]-HCID 12969325—
SolventDichloromethaneHCID 6344—
Product1-[4-(Benzyloxy)-3-methylphenyl]-2-bromoethanoneHCID 1296932770.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 1-(4-benzyloxy-3-methyl-phenyl)-ethanone (12.89 g; 53.1 mmol) in CH2Cl2 was added, dropwise, at 0° C., DIPEA (10.9 mL; 63.7 mmol) and trimethylsilyl trifluoromethanesulfonate (11.1 mL; 61.1 mmol). The resulting mixture was stirred at 0° C. for 1 hour, and subsequently, NBS (10.87 g; 61.1 mmol) was added in one portion. The mixture was allowed to warm to RT stirred overnight. Then the mixture was concentrated in vacuo, the residue dissolved in EtOAc, washed with water twice, and brine, dried (MgSO4), filtered, and concentrated in vacuo to afford 1-(4-benzyloxy-3-methyl-phenyl)-2-bromo-ethanone (11.90 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273017B2
Source datasetuspto-grants-2016_03
ORD IDord-fe1b9589b55747c4ba87726a178f5938
Source noteuspto-grants-2016_03