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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 634935Erstellt: 25. Oktober 2026

2,3,5,6-Tetrafluorophenol → tert-Butyl pentanoate

https://huagongshe.com/reaction/634935

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,3,5,6-TetrafluorophenolHCID 69858—
EduktPotassium FluorideHCID 522689—
EduktN-[(1-methyl-3-isobutyl-indole-2-cabonyl)valinyl]-3-amino-5-bromo-4-oxo-pentanoic acid, tert-butyl esterHCID 86756359—
LösungsmittelDimethylformamideHCID 6228—
Produkttert-Butyl pentanoateHCID 520048371,5%
ProduktN-[(1-methyl-3-isobutyl-indole-2-cabonyl)valinyl]-3-amino-4-oxo-5-(2,3,5,6-tetrafluorophenyloxy)-pentanoic acid, tert-butyl EsterHCID 86756358—

Reaktionsschritte

Potassium fluoride (21.6 mg, 0.37 mmol) was added to a solution of N-[(1-methyl-3-isobutyl-indole-2-carbonyl)valinyl]-3-amino-5-bromo-4-oxo-pentanoic acid, tert-butyl ester (86.1 mg, 0.149 mmol) and 2,3,5, 6-tetrafluorophenol (27.0 mg, 0.163 mmol) in DMF (2.0 ml). After stirring at room temperature for 3 hours, the reaction mixture was partitioned between ethyl acetate and water. The aqueous layer was back-extracted with ethyl acetate. The organic layers were combined, washed with saturated NaHCO3 solution, and brine, dried over sodium sulfate, and concentrated. The residue was triturated with ether to give the titled product, N-(1-methyl-3-isobutyl-indole-2-carbonyl)-valinyl-3-amino-4-oxo-5-(2,3,5,6-tetral]uorophenyloxy)-pentanoic acid, tert-butyl ester as a white solid (43.8 mg, 44%). TLC (hexane/EtOAc, 50/50): Rf=0.50.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06184244B2
Quelldatensatzuspto-grants-2001_02
ORD IDord-6da38b4177ff47fe80c51126986009bb
Quellennotizuspto-grants-2001_02