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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 273965Erstellt: 25. Oktober 2026

3-Furancarboxaldehyde, 5-(triethylsilyl)- → 4-(1-Hydroxytridecyl)-2-triethylsilylfuran

https://huagongshe.com/reaction/273965

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Furancarboxaldehyde, 5-(triethylsilyl)-HCID 10878438—
EduktHCID 178443215HCID 178443215—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-(1-Hydroxytridecyl)-2-triethylsilylfuranHCID 15663269—

Reaktionsschritte

Dodecylmagnesium bromide (a 1M solution in tetrahydrofuran; 14.3 ml; 14.3 mmol) was added dropwise to a solution of 2-triethylsilyl-4-furaldehyde (2.0 g, 9.52 mmol) in THF (20 ml) at 0 degrees C. under argon. After stirring at room temperature for 2 hours, the mixture was quenched with dilute HCl and extracted with ethyl ether. Evaporation of the dried (magnesium sulfate) extracts gave an oil, which was purified by flash chromatography on silica using 30% ethyl ether/hexane to give the titled alcohol. 1HNMR (CDCl3) 0.76 (q, 6H, J=8.0 Hz), 0.88 (t, 3H, J=6.3 Hz), 0.98 (t, 9H, J=8.0 Hz), 1.25 (m, 20H), 1.62 (d, 1H, J=4.3 Hz), 1.75 (m, 2H), 4.63 (dd, 1H, J=6.6 Hz, 1.9 Hz), 6.63 (s, 1H) and 7.57 (s, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05387606
Quelldatensatzuspto-grants-1995_02
ORD IDord-66d9dbc2c7164687bd1e6c500e1c2450
Quellennotizuspto-grants-1995_02