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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488224Generated: October 26, 2026

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

https://huagongshe.com/reaction/488224

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 numberUS05298633
Source datasetuspto-grants-1994_03
ORD IDord-ffd20763177845c492680f7c583d8759
Source noteuspto-grants-1994_03