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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 726655Erstellt: 25. Oktober 2026

2,4,5-Trichlorophenol → Cbz-D-hPro-Pro-OH

https://huagongshe.com/reaction/726655

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,4,5-TrichlorophenolHCID 7271—
EduktTriethylamineHCID 8471—
EduktDicyclohexylcarbodiimideHCID 10868—
EduktL-ProlineHCID 145742—
Edukt(2R)-1-((Benzyloxy)carbonyl)piperidine-2-carboxylic acidHCID 688346—
LösungsmittelEthyl AcetateHCID 8857—
ProduktCbz-D-hPro-Pro-OHHCID 22854903—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Cbz-D-hPro-OH (9.5 g, 36 mmol) was dissolved in ethyl acetate (100 mL) and the solution cooled to 0° C. Added to the solution was 2,4,5-trichlorophenol (7.1 g, 36 mmol) and 1,3-dicyclohexylcarbodiimide (7.4 g, 36 mmol). The reaction was stirred for 1 hour at 0° C. and 1 hour at room temperature. The precipitate was filtered and the filtrate concentrated in vacuo to an oil. The oil was dissolved in pyridine (100 mL), Pro-OH (4.2 g, 36 mmol), and triethylamine (5.0 mL, 36 mmol) were added. The reaction was stirred at room temperature (24 hours). The reaction solvent was removed in vacuo to an oil. The residue was dissolved in water (100 mL), diethyl ether (50 mL) was added and the pH adjusted to 9.5 with 2N sodium hydroxide. The aqueous layer extracted twice with diethyl ether. The aqueous layer separated, the pH adjusted to 2.8 with 3N hydrochloric acid and ethyl acetate (150 mL) was added. The organic layer was separated, dried (MgSO4), and the filtrate evaporated in vacuo to an amorphous solid (11.4 g, 88%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05710130
Quelldatensatzuspto-grants-1998_01
ORD IDord-4f15455e5bda4e229be67e140928d4fb
Quellennotizuspto-grants-1998_01