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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1770328Generated: October 26, 2026

Allyl chloride → 4,4-Dichloro-2-phenyl-4-silaheptane

https://huagongshe.com/reaction/1770328

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl chlorideHCID 7850—
ReactantSilaneHCID 23953—
ReactantTrichloro(2-phenylpropyl)silaneHCID 12887569—
Reactant1,4,4-Trichloro-6-phenyl-4-silaheptaneHCID 15217570—
Reactant3-Phenyl-1,1-dichloro-1-silabutaneHCID 123324342—
CatalystChloroplatinic acidHCID 61859—
Product4,4-Dichloro-2-phenyl-4-silaheptaneHCID 15217571—

Reaction Steps

To a 500 ml, three neck, round bottomed flask equipped with a mechanical stirrer, a dropping funnel, and a reflux condenser, 6.0 g (0.03 mole) of 3-phenyl-1,1-dichloro-1-silabutane, 6.28 g (0.09 mole) of allyl chloride, and 150 μl of 1% chloroplatinic acid in isopnopanol were placed under the dry nitrogen atmosphere. The flask was then immersed in a hot water bath of 45°-50° C. The solution was stirred vigorously for three hours. Gas chromatography analysis showed that no silane was Left. Vacuum distillation of the solution gave 2.21. g (bp, 111°-2° C./0.6 mmHg) of 1,4,4-trichloro-6-phenyl-4-silaheptane and 2.63 g of 3-phenyl-1,1,1-trichloro-1-silabutane. Besides these products, a small amount of 4,4-dichloro-2-phenyl-4-silaheptane was also obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05386050
Source datasetuspto-grants-1995_01
ORD IDord-05421f19eae94c13807805b87ab69b7f
Source noteuspto-grants-1995_01