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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493460Generated: October 25, 2026

Trichloro-2-propen-1-ylsilane → HCID 57681726, compound

https://huagongshe.com/reaction/493460

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloro-2-propen-1-ylsilaneHCID 7867—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant(3R,4R)-2,5-dimethoxy-2,5-dimethyl-hexane-3,4-diolHCID 11218000—
SolventDichloromethaneHCID 6344—
ProductHCID 57681726HCID 5768172644.5%

Reaction Steps

Preparation of (4R,5R)-2-allyl-2-chloro-4,5-bis-(1-methoxy-1-methyl-[1,3,2]dioxasilolane: To a cooled (0° C.) solution of allyltrichlorosilane (7.0 mL; 48 mmol) in CH2Cl2 (80 mL) was added 1,8-diazabicyclo[5.4.0]undec-7-ene (15 mL; 102 mmol). A solution of (3R,4R)-2,5-dimethoxy-2,5-dimethyl-hexane-3,4-diol (10.0 g; 48 mmol) in CH2Cl2 (80 mL) was then added and the mixture was allowed to warm to ambient temperature and stirred for 12 hours. The solution was concentrated and the residue was treated with diethylether (100 mL). The mixture was stirred for 1 hour. The mixture was then filtered and the filtrate was concentrated. The residue was distilled under reduced pressure to give 6.6 g (44%) of (4R,5R)-2-allyl-2-chloro-4,5-bis-(1-methoxy-1-methyl-ethyl)-[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-75b0dd9355294c39a606712ebada1dd7
Source noteuspto-grants-2009_05