Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489412Generated: October 25, 2026

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

https://huagongshe.com/reaction/1489412

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, CH2CH2CO2), 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=O), 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 numberUS05677440
Source datasetuspto-grants-1997_10
ORD IDord-32658d8b714645e08b44cb050dc07e41
Source noteuspto-grants-1997_10