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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1699803Generated: October 26, 2026

Chlorotrimethylsilane → 1-(2,4-Dichlorophenyl)-1-trimethylsilyloxyethene

https://huagongshe.com/reaction/1699803

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantDiisopropylamineHCID 7912—
Reactant2',4'-DichloroacetophenoneHCID 16693—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexamethylphosphoramideHCID 12679—
Product1-(2,4-Dichlorophenyl)-1-trimethylsilyloxyetheneHCID 22388270—

Reaction Steps

Diisopropylamine (16.2 g) was dissolved in tetrahydrofuran (133 ml), and 1.6N n-butyl lithium (100 ml) was dropwise added thereto under ice-cooling. The reaction mixture was stirred at the same temperature for 10 min, and a solution of 2,4-dichoroacetophenone (25.2 g) in tetrahydrofuran (133 ml) was dropwise added under cooling in a dry ice-acetone bath. Hexamethylphosphoramide (26.7 ml) was added little by little. The mixture was stirred at the same temperature for 5 min, and chlorotrimethylsilane (20.3 ml) was dropwise added, which was followed by stirring at room temperature for 30 min. The reaction mixture was partitioned between ice-cooled n-hexane and ice-cooled water. The organic layer was washed twice with ice-cooling water and then once with saturated brine, dried over sodium sulfate and concentrated under reduced pressure to dryness to give a crude product (37.5 g) of the objective compound as a pale-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06348474B1
Source datasetuspto-grants-2002_02
ORD IDord-c88909ed16f6428a9a7ed6f76d5ca747
Source noteuspto-grants-2002_02