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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1456908Erstellt: 24. Oktober 2026

Dicyclohexylcarbodiimide → Pentafluorophenyl N-tert-butoxycarbonyl-6-aminohexanoate

https://huagongshe.com/de/reaction/1456908

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDicyclohexylcarbodiimideHCID 10868—
EduktPentafluorophenolHCID 13041—
Edukt6-((tert-Butoxycarbonyl)amino)hexanoic acidHCID 637602—
LösungsmittelEthyl AcetateHCID 8857—
ProduktPentafluorophenyl N-tert-butoxycarbonyl-6-aminohexanoateHCID 309147994%

Reaktionsschritte

To a solution of N-Boc-6-aminohexanoic acid (4.78 g, 20.8 mmol) and pentafluorophenol (3.68 g, 20 mmol) in 50 mL of EtOAc was added DCC (4.12 g, 20 mmol). This was allowed to stir for 16 h, and was then filtered and the filtrate evaporated in vacuo to a syrup. On standing, this crystallized to give 7.46 g (94%) of the ester. Rerystallization from isopropanol/1% acetic acid gave 6.26 g of white needles, mp 81°-83° C. 1H NMR (CDCl3) δ 1.4-1.6 (m, 15H, Boc CH3 and internal CH2), 1.8 (m, 2H, C2CH2CO2), 2.67 (5, J=7.3 Hz, 2H, CH2CO2), 3.1 (m, 2H, NHCH2), 4.5 (b, 1H, NH). 13C NMR (CDCl3) δ 24.38 (C4), 26.00 (C3), 28.39 (Boc CH3), 29.70 (C5), 33.20 (C2), 40.28 (C6), 79 (Boc C), 156 (Boc C=0), 169 (C1). Anal. Calcd for C17H20NO4F5 : C, 51.4; H, 5.1; N, 3.5. Found: C, 51.5; H, 5.0; N, 3.4.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05846728
Quelldatensatzuspto-grants-1998_12
ORD IDord-de2e1a80682d44898fff4a6c993cef4a
Quellennotizuspto-grants-1998_12