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HRID 1953175Erstellt: 26. Oktober 2026

3,3,3-Trifluoropropyl-trimethoxysilane → Piperidine, 1-[dimethoxy(3,3,3-trifluoropropyl)silyl]-2-ethyl-

https://huagongshe.com/reaction/1953175

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3,3,3-Trifluoropropyl-trimethoxysilaneHCID 67933—
Edukt2-EthylpiperidineHCID 94205—
EduktHCID 178418918HCID 178418918—
Edukt2-Ethylpiperdinylmagnesium chlorideHCID 178436343—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktPiperidine, 1-[dimethoxy(3,3,3-trifluoropropyl)silyl]-2-ethyl-HCID 1126654388%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

Following the same general procedure described on Example 1, a flask was charged with one mol (218 gm) of 3,3,3-trifluoropropyltrimethoxysilane was added to one mol of 2-ethylpiperdinylmagnesium chloride, the salt having been prepared in situ by adding 2-ethylpiperidine (120 g, 1.05 mol) to isopropylmagnesium chloride (1 mol) in 500 ml of tetrahydrofuran. The reaction was mildly exothermic and the temperature rose to 45° C. at the end of the addition time of one hour. The reaction mixture was refluxed at the pot temperature of 70° C. for one hour and then cooled to room temperature. The 3,3,3-trifluoropropyl(2-ethylpiperidino)dimethoxysilane was filtered under nitrogen atmosphere from the magnesium methoxychloride. The filter cake was washed with ether (2×200 ml) to obtain the residual product. The solvent was removed by distillation to a pot temperature of 100° C. The residue was distilled under vacuum to yield 263 g of 3,3,3-trifluoropropyl(2-ethylpiperidino)dimethoxysilane as a colorless oil (purity>98%); bp 70° C./0.1 mm. The total yield was 88% of theoretical.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06114558
Quelldatensatzuspto-grants-2000_09
ORD IDord-2a799657f9bc46a9bbdcd5af5672a57c
Quellennotizuspto-grants-2000_09