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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1274508Generated: October 26, 2026

Iodine → tert-Butyldiphenylchlorosilane

https://huagongshe.com/reaction/1274508

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantDichlorodiphenylsilaneHCID 6627—
Reactanttert-BUTYL CHLORIDEHCID 10486—
ReactantMagnesiumHCID 5462224—
ReactantHCID 178418310HCID 178418310—
CatalystCopper, bis(2,4-pentanedionato-O,O')-, (SP-4-1)-HCID 5363992—
Solvent1,2-DimethoxyethaneHCID 8071—
Producttert-ButyldiphenylchlorosilaneHCID 9407885%

Reaction Conditions

Temperature70 °C

Reaction Steps

48.6 g (2.0 mol) of magnesium filings and a spatula-tip of iodine are initially introduced into a 2 1 three-necked flask with a precision glass stirrer, straight enclosed-scale thermometer, Dimroth condenser and dropping funnel under a blanket of inert gas. By addition of 600 ml of ethylene glycol dimethyl ether and 203.7 g (2.2 mol) of tert-butyl chloride, tert-butylmagnesium chloride is prepared. Initially 5.2 g (0.02 mol) of copper(II) acetylacetonate and then, at 50° C. over 2 hours, 455.8 g (1.8 mol) of diphenyldichlorosilane are subsequently added dropwise. The internal temperature of the flask rises slightly, and the mixture is subsequently stirred at 70° C. for a further 3 hours to bring the reaction to completion. To remove the precipitated magnesium salt from the solution, the reaction mixture is filtered through a pressure suction filter maintained under an argon atmosphere. The filter cake is rinsed with ethylene glycol dimethyl ether. A concluding fractional distillation of the combined filtrates in vacuo gives 420.6 g of tert-butyldiphenylchlorosilane (85% yield, based on the diphenyldichlorosilane) as a colorless liquid in a GC purity of 92%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06156918
Source datasetuspto-grants-2000_12
ORD IDord-cbde98aec9034104afcedb1ef2902e1d
Source noteuspto-grants-2000_12