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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181754Generated: October 27, 2026

Iodine → (6S)-3-iodo-6-(6-quinolyl)-6-(triethylsilyloxy)-3-hexene

https://huagongshe.com/reaction/2181754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
ReactantTriphenyl(propyl)phosphonium iodideHCID 10982905—
Reactant(3S)-3-(triethylsilyloxy)-3-(6-quinolyl)propanalHCID 86586607—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product(6S)-3-iodo-6-(6-quinolyl)-6-(triethylsilyloxy)-3-hexeneHCID 86587399—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A suspension of propyltriphenylphosphonium iodide (8.2 gm) in 150 mL of tetrahydrofuran is treated with a 2.5 M solution of n-butyllithium (7.17 mL) at ambient temperature. The resulting red solution is transferred via cannula into a vigorously stirred solution of iodine (4.54 gm) in 150 mL of tetrahydrofuran cooled to −78° C. The resulting suspension is stirred for 5 minutes, then gradually warmed to −30° C. A 1.0 M solution of sodium hexamethyldisilazide (17.3 mL) is then added dropwise to form a red solution. A solution of (3S)-3-(triethylsilyloxy)-3-(6-quinolyl)propanal (1.9 gm) in 10 mL of tetrahydrofuran is then added dropwise, and stirring is continued at −30° C. for 30 minutes. The mixture is diluted with ether, filtered through a pad of Celite, and concentrated. The product is purified by flash chromatography on silica gel.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06893859B2
Source datasetuspto-grants-2005_05
ORD IDord-9a572146f6c349df8fa5ca8bbd67a359
Source noteuspto-grants-2005_05