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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371310Generated: October 27, 2026

Iodine → Allyl(chloromethyl)[bis(4-fluorophenyl)]silane

https://huagongshe.com/reaction/371310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantAllyl bromideHCID 7841—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesiumHCID 5462224—
ReactantChloro(chloromethyl)[bis(4-fluorophenyl)]silaneHCID 13392398—
SolventDiethyl EtherHCID 3283—
ProductAllyl(chloromethyl)[bis(4-fluorophenyl)]silaneHCID 13489944—

Reaction Steps

A mixture of 1.04 g (0.0428 mol) of magnesium turnings and about 0.05 g of iodine in 50 ml of ether was stirred under nitrogen while a solution of 4.7 ml (0.0544 mol) of 3-bromopropene in ether was added dropwise. The iodine color quickly disappeared, and the reaction temperature was kept around 30° C. by cooling with ice-water. The resulting solution was stirred 2 hours at room temperature. A solution of 10.0 gm (0.033 mol) of bis(4-fluorophenyl)chlorochloromethylsilane in 20 ml of ether was then added over 5 minutes, and the resulting mixture was allowed to stir overnight. The solution was treated with 20 ml of saturated aqueous ammonium chloride and extracted with ether. The ether was washed with water and with brine. Drying over magnesium sulfate and removal of solvent afforded a clear colorless oil which was distilled at 0.4 torr (bp 120°-130° C.) to give the title compound: nmr (CDCl3) 2.3 (2H, d, J=8 Hz), 3.3 (1H, s), 5.0 (2H, m), 5.8 (1H, m), 7.1 (4H, t, J=9 Hz), 7.6 (4H, d of d, J=9,6 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04530922
Source datasetuspto-grants-1985_07
ORD IDord-d4debc089f1b48cb9779ca6c4e512cde
Source noteuspto-grants-1985_07