반응 #53408

ord-4a2186cd1db345cfbc7dd8289da03907

반응 방정식

COCCBr
2-bromoethyl methyl ether
O=C(NCCCCc1ccc(O)cc1)OCc1ccccc1
29
O=C(NCCCCc1ccc(O)cc1)OCc1ccccc1
N-Cbz-4-(4-Hydroxyphenyl)butylamine
[H-].[Na+]
sodium hydride
COCCOc1ccc(CCCCNC(=O)OCc2ccccc2)cc1
64
수율 66.7%
COCCOc1ccc(CCCCNC(=O)OCc2ccccc2)cc1
N-Cbz-4-[4-(1,4-Dioxapent-1-yl)phenyl]butylamine
수율 66.7%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGthe mixture was stirred at room temperature overnight
  2. 2
    기타The solvent was removed under reduced pressure
  3. 3
    기타the material was purified by column chromatography (silica gel, 10:1 methylene chloride/ethyl acetate)

실험 절차

To a vigorously stirred solution of 29 (4 g, 0.013 mol) in anhydrous THF (150 mL) under nitrogen at 0° C. was added sodium hydride (60% dispersion in mineral oil, 0.64 g, 0.016 mol). The mixture was stirred for 15 min then tetrabutylammonium iodide (0.5 g, 0.0013 mol) and 2-bromoethyl methyl ether (2.04 g, 0.015 mol) were added and the mixture was stirred at room temperature overnight. The solvent was removed under reduced pressure and the material was purified by column chromatography (silica gel, 10:1 methylene chloride/ethyl acetate) to provide 64 (3.1 g, 64%). 1H NMR (300 MHz, CDCl3) δ 1.60 (m, 4H), 2.59 (m, 2H), 3.23 (m, 2H), 3.45 (s, 3H), 3.77 (m, 2H), 4.10 (m, 2H), 5.13 (s, 2H), 6.88 (d, 2H), 7.08 (d, 2H), 7.47 (s, 5H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06858615B2uspto-grants-2005_02