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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 493388Erstellt: 26. Oktober 2026

Acetic Anhydride → HCID 178482205, Verbindung

https://huagongshe.com/reaction/493388

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AnhydrideHCID 7918—
EduktTriethylamineHCID 8471—
EduktEthyl AcetateHCID 8857—
EduktHCID 178507748HCID 178507748—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 178482205HCID 178482205—

Reaktionsschritte

4-{4-[2-(phenoxymethyl)-1H-imidazol-4-yl]phenoxy}aniline (238 mg, 0.0066 mol), (prepared according to a method analogous to that described in Example 28) is suspended in dichloromethane (5 ml) at 23° C. Triethylamine (0.1 ml, 0.0079 mol) and acetic anhydride (0.062 ml, 0.0066 mol) are added. The mixture is then stirred for 20 hours then evaporated to dryness. The oil obtained is taken up with ethyl acetate and water. After decantation and extraction by ethyl acetate, the organic phase is washed with water then with a saturated solution of sodium chloride, dried over sodium sulphate then the solvent is evaporated off. The residue obtained is adsorbed on silica then purified by chromatography on a Biotage-type silica column (eluent: ethyl acetate-heptane: 7-3 to 9-1). After washing with diisopropyl ether and isopentane, a beige-coloured powder is obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07534805B2
Quelldatensatzuspto-grants-2009_05
ORD IDord-84812724710249d4b3aac5f37c78b811
Quellennotizuspto-grants-2009_05