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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1681515Generated: November 4, 2026

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

https://huagongshe.com/reaction/1681515

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 numberUS05171863
Source datasetuspto-grants-1992_12
ORD IDord-1311c4d139614cfc93e278371cd7def5
Source noteuspto-grants-1992_12