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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1456908Generated: October 25, 2026

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

https://huagongshe.com/reaction/1456908

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantPentafluorophenolHCID 13041—
Reactant6-((tert-Butoxycarbonyl)amino)hexanoic acidHCID 637602—
SolventEthyl AcetateHCID 8857—
ProductPentafluorophenyl N-tert-butoxycarbonyl-6-aminohexanoateHCID 309147994%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05846728
Source datasetuspto-grants-1998_12
ORD IDord-de2e1a80682d44898fff4a6c993cef4a
Source noteuspto-grants-1998_12