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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050641Generated: October 30, 2026

5-(Trimethylsilyl)furan-3-carbaldehyde → 3-(1-Hydroxytridecyl)-5-trimethylsilylfuran

https://huagongshe.com/reaction/2050641

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(Trimethylsilyl)furan-3-carbaldehydeHCID 15663251—
ReactantHCID 178443215HCID 178443215—
SolventTetrahydrofuranHCID 8028—
Product3-(1-Hydroxytridecyl)-5-trimethylsilylfuranHCID 15663268—

Reaction Steps

A solution of 2-trimethylsilyl-4-furaldehyde (0.5 g, 2.97 mmol) in tetrahydrofuran (5 ml) was added to a solution of dodecyl magnesium bromide (5.95 mmol; prepared from 1.48 g dodecyl bromide and 146 mg magnesium turnings in 30 ml tetrahydrofuran) at room temperature. After 2 hours, the mixture was quenched with ammonium chloride solution and extracted thoroughly with ethyl ether. Evaporation of the dried (magnesium sulfate) extracts gave an oil which was flash chromatographed on silica using 10% ethyl ether/hexane. Fractions with Rf about 0.13 gave, after evaporation, the title alcohol as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05013850
Source datasetuspto-grants-1991_05
ORD IDord-83c2c68832544c0fa2b37b4972222448
Source noteuspto-grants-1991_05