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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345891Generated: October 26, 2026

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

https://huagongshe.com/reaction/345891

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° 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 numberUS05059611
Source datasetuspto-grants-1991_10
ORD IDord-c70f000417f641b2925d2d3d94cd306b
Source noteuspto-grants-1991_10