Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 433034Erstellt: 25. Oktober 2026

Triphenylphosphine → HCID 178512850, Verbindung

https://huagongshe.com/reaction/433034

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphenylphosphineHCID 11776—
EduktDiisopropylcarbodiimideHCID 12734—
Edukt1-HydroxybenzotriazoleHCID 75771—
Edukt4-Bromo-3,5-dihydroxybenzoic acidHCID 86023—
Edukt2,4-Dichlorophenethyl alcoholHCID 2734099—
EduktDiisopropyl azodicarboxylateHCID 5363146—
EduktHCID 178454311HCID 178454311—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 178512850HCID 178512850—

Reaktionsschritte

Rink resin (500 mg; loading 0.3 mmol/g) functionalized with Arg(Boc)2 was coupled with 176 mg of 3,5-dihydroxy-4-bromobenzoic acid in the presence of DIC (110 mg) and HOBt (78 mg) in DMF. The resin was then washed and treated with a 30% solution of benzyltrimethylammonium hydroxide in DMF for 1 h. The resin was washed with DMF, 10% acetic acid in DMF, DMF, and DCM and dried in vacuo for 3 h. The dried resin was washed with anhydrous THF and mixed with 0.2 mmol of triphenylphosphane and 0.2 mmol of 2-(2,4-dichlorophenyl)ethanol in 2 ml of dry THF. The suspension of the resin was cooled in a refrigerator for 16 min and 50 μl (0.2 mmol) of DIAD in 0.5 ml of dry THF were added. Coupling was continued overnight at room temperature. The resin was washed with dry THF and the coupling was repeated for additional 8 h. The resin was washed and dried, and the final product was cleaved off and processed as described in Example 1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06664393B2
Quelldatensatzuspto-grants-2003_12
ORD IDord-6b819f116e134274b935d0f22d796e7d
Quellennotizuspto-grants-2003_12