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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068516Generated: October 26, 2026

Allyl chloride → Trichloro-2-propen-1-ylsilane

https://huagongshe.com/reaction/1068516

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl chlorideHCID 7850—
ReactantTriphenylphosphineHCID 11776—
ReactantTrichlorosilaneHCID 24811—
CatalystCuprous chlorideHCID 62652—
ProductTrichloro-2-propen-1-ylsilaneHCID 786720%
ProductPropyltrichlorosilaneHCID 885020%
Product1,3-Bis(trichlorosilyl)propaneHCID 1124385617%

Reaction Steps

In the same apparatus and procedure as Example 1 above, 0.037 g (0.14 mmol) of triphenylphosphine, 1.4 mg (0.014 mmol) of CuCl, 1.07 g (14.0 mmol) of allyl chloride, and 9.48 g (70.0 mmol) of trichlorosilane were reacted at 150° C. for 10 hrs. The resulting mixture was distilled to give 0.5 g of allytrichlorosilane (bp; 117-8° C., yield; 20%), 0.51 g of propyltrichlorosilane (bp; 123-5° C., yield; 20%), and 0.73 g of 1,3-bis(trichlorosilyl)propane (bp; 88-90° C./12.5 mmHg, yield; 17%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06251057B1
Source datasetuspto-grants-2001_06
ORD IDord-2eea8f0e151d477caf73a5c824033852
Source noteuspto-grants-2001_06