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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65505Generated: October 25, 2026

Allyl chloride → (3-Chloropropyl)(triethyl)silane

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Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl chlorideHCID 7850—
ReactantTriethylsilaneHCID 12052—
ReactantTrichlorosilaneHCID 24811—
Product(3-Chloropropyl)(triethyl)silaneHCID 1256678440.9%

Reaction Conditions

Temperature65 °C

Reaction Steps

In a 100 ml apparatus, there were combined 11.6 g (0.1 mol) of Et3SiH, 1.7 g (0.0125 mol) of Cl3SiH and 0.05 ml of Pt catalyst solution. The mixture was heated to 65° C. and addition of 7.7 g (0.1 mol) of allyl chloride begun. There was an exothermic reaction to 108.5° C. over 16 min, followed by a temperature drop. Addition of allyl chloride was complete in 31 min, with heat then applied at reflux (up to 114° C.) over 170 min. Vacuum distillation yielded 7.88 g (40.9%) of Et3SiCH2CH2CH2Cl with a Et3SiCH2CH2CH2Cl/Et3SiCl selectivity ratio of 1.13. This example shows that this sequence of combination of reactants allows the Cl3SiH promoter to be consumed, at which point the reaction of Et3SiH with allyl chloride proceeds at the low rate and selectivity exhibited in Comparative Example DD.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04614812
Source datasetuspto-grants-1986_09
ORD IDord-4de9006738214215a53917a7083e555b
Source noteuspto-grants-1986_09