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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396572Generated: November 1, 2026

Chlorotrimethylsilane → HCID 55273228, compound

https://huagongshe.com/reaction/1396572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethyl borateHCID 9009—
Reactant4-Bromo-2-chloro-6-fluorophenolHCID 2773270—
ReactantAcetone cardiceHCID 18522661—
SolventTetrahydrofuranHCID 8028—
ProductHCID 55273228HCID 55273228—

Reaction Steps

4-Bromo-2-chloro-6-fluoro-phenol (0.500 g, 2.21 mmol) is dissolved in dry THF, the reaction mixture is cooled to −78° C. (dry-ice/acetone bath) and 2.5M n-butylithium (1.06 ml, 2.66 mmol) is slowly added drop wise with stirring for 5 minutes. TMSCl (0.298 ml, 2.33 mmol) is added drop wise maintaining the temperature below −70° C. and the reaction mixture is stirred for 30 minutes. Boric acid triethyl ester is then added (0.385 ml, 2.26 mmol) followed by the second addition of n-butylitlium (1.06 ml, 2.66 mmol) maintaining the temperature below −65° C. The reaction mixture is stirred at −70° C. for 30 minutes then quenched with 5M HCl (5 ml) and allowed to warm to room temperature with stirring for 30 minutes. The reaction mixture is diluted with water and EtOAc and the organic portion is washed with 5M NaOH. The aqueous layer is acidified with 5M HCl and extracted with EtOAc, this organic portion is washed with brine, dried over MgSO4 and concentrated in vacuo to afford the title compound as an off white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901134B2
Source datasetuspto-grants-2014_12
ORD IDord-b061f92259704ae9bfffd8cc0e882292
Source noteuspto-grants-2014_12