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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351353Generated: October 25, 2026

Chlorotrimethylsilane → 1,2-Difluoro-3-trimethylsilylbenzene

https://huagongshe.com/reaction/351353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
Reactant1,2-DifluorobenzeneHCID 9706—
Reactanttert-Butyl methyl etherHCID 15413—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1,2-Difluoro-3-trimethylsilylbenzeneHCID 10899371—

Reaction Steps

625 ml (1 mol) of 1.6 M BuLi are added dropwise at −78° C. to a solution of 114 g (1 mol) of 1,2-difluorobenzene in 1 l of dry tetrahydrofuran. After 1 hour, 140 ml (120 g, 1.1 mol) of trimethylsilyl chloride are slowly added dropwise at −78° C. The mixture is allowed to warm to room temperature overnight, and then 200 ml of methyl tert-butyl ether and 200 ml of water are added. The organic phase is washed with water (2×100 ml) and sat. NaCl (1×100 ml) and dried using magnesium sulfate, and the solvent is removed under reduced pressure. 170 g (91%) of 5 distil over from the residue at from 100 to 102° C./70 mbar.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07183447B2
Source datasetuspto-grants-2007_02
ORD IDord-5b4a85235cc44b289503edb92ef623ce
Source noteuspto-grants-2007_02