Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181757Generated: October 26, 2026

Iodine → HCID 86586614, compound

https://huagongshe.com/reaction/2181757

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant(3r)-3-(Triethylsilyloxy)-3-(6-quinolyl)propanalHCID 87867747—
ReactantButyllithiumHCID 178418339—
CatalystEthyltriphenylphosphonium iodideHCID 78474—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86586614HCID 86586614—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A suspension of ethyltriphenylphosphonium iodide (7.9 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 (3R)-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-633d665acf8d4d9a903b9125b4c2cf7f
Source noteuspto-grants-2005_05