HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 985735Generated: October 30, 2026
Allyl chloride → (3-Chloropropyl)triethoxysilane
https://huagongshe.com/reaction/985735
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl chloride | HCID 7850 | — |
| Reactant | Triethoxysilane | HCID 13830 | — |
| Reactant | Trimethoxysilane | HCID 17215 | — |
| Catalyst | Ruthenium | HCID 23950 | — |
| Product | (3-Chloropropyl)triethoxysilane | HCID 78771 | 41% |
Reaction Steps
Ruthenium has been reported to be a very efficient catalyst for the hydrosilation reaction of allyl chloride and trimethoxysilane. Japanese Patent No. 2,976,011 discloses the Ru-catalyzed hydrosilation reaction of triethoxysilane and allyl chloride to give chloropropyltriethoxysilane in about 41% yield. U.S. Pat. No. 5,559,264 describes the hydrosilation reaction of a methoxysilane and allyl chloride in the presence of a ruthenium catalyst and preferably in the substantial absence of solvent to provide a chloroalkylalkoxysilane. Tanaka et al., J. Mol. Catal. 1993, 81, 207-214 report the ruthenium carbonyl-catalyzed hydrosilation reaction of trimethoxysilane and allyl chloride and Japanese Patent Application No. 8[1996]-261232 describes the activation of ruthenium carbonyl for use as a hydrosilation catalyst for the same reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06872845B2 |
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| Source dataset | uspto-grants-2005_03 |
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| ORD ID | ord-9cf4cf866dfa4e5bbebde78334840aed |
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| Source note | uspto-grants-2005_03 |
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