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HRID 1456908作成日:2026年10月26日

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

https://huagongshe.com/reaction/1456908

反応式

関与物質

役割名称HCID仕込み量
反応物DicyclohexylcarbodiimideHCID 10868—
反応物PentafluorophenolHCID 13041—
反応物6-((tert-Butoxycarbonyl)amino)hexanoic acidHCID 637602—
溶媒Ethyl AcetateHCID 8857—
生成物Pentafluorophenyl N-tert-butoxycarbonyl-6-aminohexanoateHCID 309147994%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05846728
出典データセットuspto-grants-1998_12
ORD IDord-de2e1a80682d44898fff4a6c993cef4a
出典メモuspto-grants-1998_12