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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 348251Erstellt: 23. Oktober 2026

Iodine → HCID 86586614, Verbindung

https://huagongshe.com/de/reaction/348251

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktSodium bis(trimethylsilyl)amideHCID 2724254—
Edukt(3r)-3-(Triethylsilyloxy)-3-(6-quinolyl)propanalHCID 87867747—
EduktButyllithiumHCID 178418339—
KatalysatorEthyltriphenylphosphonium iodideHCID 78474—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 86586614HCID 86586614—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07176235B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-fb07d3d7e0b74beeaa477216b98be3b2
Quellennotizuspto-grants-2007_02