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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493459Generated: October 27, 2026

2-Allyl-2-chloro-4,4,5,5-tetramethyl-[1,3,2]dioxasilolane → 2-Allyl-4,4,5,5-tetramethyl-2-vinyloxy-[1,3,2]dioxasilolane

https://huagongshe.com/reaction/493459

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Allyl-2-chloro-4,4,5,5-tetramethyl-[1,3,2]dioxasilolaneHCID 57681722—
ReactantTrimethylvinyloxysilaneHCID 101265072—
ReactantHCID 178418348HCID 178418348—
SolventPentaneHCID 8003—
Product2-Allyl-4,4,5,5-tetramethyl-2-vinyloxy-[1,3,2]dioxasilolaneHCID 1119554272.3%

Reaction Steps

To a cooled (0° C.) solution of MeLi (16.2 mL; 23 mmol; 1.4 M in Et20) was added trimethylvinyloxysilane (2.7 g; 23 mmol). The solution was warmed to room temperature and was stirred for 1 hour. The solution was cooled to −78° C., and 2-allyl-2-chloro-4,4,5,5-tetramethyl-[1,3,2]dioxasilolane (5.5 g; 25 mmol) was added. The solution was warmed to room temperature and stirred for 2 hours. The solution was diluted with pentane (20 mL), and the mixture was then filtered through a pad of celite. The filtrate was concentrated, and the residue was distilled under reduced pressure to give 3.8 g (70%) of 2-allyl-4,4,5,5-tetramethyl-2-vinyloxy-[1,3,2]dioxasilolane as a clear, colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07534905B2
Source datasetuspto-grants-2009_05
ORD IDord-39a427f8a7a24e40bba5fb4f4b9d73fc
Source noteuspto-grants-2009_05