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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029378Generated: October 25, 2026

3,3,3-Trifluoropropyl-trimethoxysilane → 3,3,3-Trifluoropropyl(isobutyl)dimethoxy silane

https://huagongshe.com/reaction/1029378

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,3,3-Trifluoropropyl-trimethoxysilaneHCID 67933—
ReactantSilane hexaneHCID 131717238—
ReactantHCID 178418368HCID 178418368—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
Product3,3,3-Trifluoropropyl(isobutyl)dimethoxy silaneHCID 19900042—

Reaction Steps

Under nitrogen, a 500 ml Schlenk flask was cooled to room temperature and charged with 150 ml of diethyl ether and isobutylmagnesium chloride (0.06 mol, 30.24 ml). This was stirred and heated slightly to 30° C. A second Schlenk flask (100 ml) was purged with nitrogen to room temperature and charged with 75 ml hexane and 3,3,3-trifluoropropyltrimethoxy silane (0.0504 mol, 10 ml) and stirred. The silane/hexane solution was added dropwise via cannula to the Grignard/diethyl ether mixture producing a white precipitate midway through the addition. After addition (1.25 hrs.), the reaction mixture was stirred at room temperature for one hour. The flask was fitted with a reflux condenser and the reaction mixture was refluxed for two hours, then allowed to cool to room temperature. The reaction mixture was filtered through a medium porosity frit, using Celite diatomaceous earth and glass wool as a filtering aid. The solids collected weighed 7.55 g (theoretical=4.56 grams of magnesium salts). The slightly cloudy filtrate was kept under nitrogen overnight.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05102842
Source datasetuspto-grants-1992_04
ORD IDord-25c09710342543ffa93dee71783fd183
Source noteuspto-grants-1992_04