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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273965Generated: October 25, 2026

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

https://huagongshe.com/reaction/273965

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Furancarboxaldehyde, 5-(triethylsilyl)-HCID 10878438—
ReactantHCID 178443215HCID 178443215—
SolventTetrahydrofuranHCID 8028—
Product4-(1-Hydroxytridecyl)-2-triethylsilylfuranHCID 15663269—

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05387606
Source datasetuspto-grants-1995_02
ORD IDord-66d9dbc2c7164687bd1e6c500e1c2450
Source noteuspto-grants-1995_02