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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2279450Generated: November 1, 2026

Ammonium Chloride → Ethanone, 1-(4-chloro-3-fluorophenyl)-2-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-

https://huagongshe.com/reaction/2279450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant2-(tert-butyldimethylsilyloxy)-N-methoxy-N-methylacetamideHCID 11601094—
ReactantHCID 178505943HCID 178505943—
SolventTetrahydrofuranHCID 8028—
ProductEthanone, 1-(4-chloro-3-fluorophenyl)-2-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-HCID 6829440893.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 60 (15.12 g, 64.79 mmol) and THF (50 mL) cooled to 0° C. was added dropwise (4-chloro-3-fluorophenyl)magnesium bromide (226.8 mL, 113.4 mmol) and the solution was stirred at 0° C. for 2 h. Saturated NH4Cl was added and the reaction was extracted with DCM. The organic layer was separated, dried, filtered and concentrated. The crude product was purified by passage through a SiO2 plug eluting with 5% EtOAc/hexane to afford 18.36 g (93.6%) of 2-(tert-butyldimethylsilyloxy)-1-(4-chloro-3-fluorophenyl)ethanone (62).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133187B2
Source datasetuspto-grants-2015_09
ORD IDord-d5290904d5624326901fbd297282c949
Source noteuspto-grants-2015_09