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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257357Generated: November 2, 2026

Sodium Thiosulfate → 2-bromo-1-(3-{[tert-butyl(dimethyl)silyl]oxy}phenyl)ethanone

https://huagongshe.com/reaction/1257357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactant1-(3-{[tert-Butyl(dimethyl)silyl]oxy}phenyl)ethan-1-oneHCID 14361489—
ReactantPhenyltrimethylammonium bromide dibromideHCID 17977687—
SolventDiethyl EtherHCID 3283—
Product2-bromo-1-(3-{[tert-butyl(dimethyl)silyl]oxy}phenyl)ethanoneHCID 11645608—

Reaction Steps

To a solution (40 mL) of the compound (9.4 g, 37 mmol) obtained in Example 38a in diethyl ether was added phenyltrimethylammonium tribromide (14 g, 37 mmol), and the mixture was stirred at room temperature for 5 hr. After confirmation of the termination of the reaction by TLC, aqueous sodium thiosulfate solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The obtained organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to give a crude title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461348B2
Source datasetuspto-grants-2013_06
ORD IDord-54a7c394510e48d29995ed5f9065b186
Source noteuspto-grants-2013_06