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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109884Generated: November 1, 2026

Dodecanal → 4-(5-Hydroxy-3-hexadecynyl)-2-triethylsilylfuran

https://huagongshe.com/reaction/1109884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDodecanalHCID 8194—
Reactant4-(4,4-Dibromo-3-butenyl)-2-triethylsilylfuranHCID 15037105—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product4-(5-Hydroxy-3-hexadecynyl)-2-triethylsilylfuranHCID 15037106—

Reaction Steps

n-Butyl lithium (a 2.5M solution in tetrahydrofuran; 0.42 ml, 1.04 mmol) was added dropwise to a solution of 4-(4,4-dibromo-3-butenyl)-2-triethylsilylfuran (200 mg, 0.51 mmol) in tetrahydrofuran (8 ml) at -78 degrees under argon. After 2 hours, a solution of 1-dodecanal (102 mg, 0.56 mmol) in tetrahydrofuran (1 ml) was added. Stirring was continued for 14 hours, while the cooling bath attained room temperature. The mixture was quenched with water and was extracted with ethyl ether. Evaporation of the dried (magnesium sulfate) extracts gave a residue, which was purified by a silica column with 15% ethyl ether/hexane to give the titled alcohol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05322953
Source datasetuspto-grants-1994_06
ORD IDord-142a973d50894237839980ccf72f19b7
Source noteuspto-grants-1994_06