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Cyclobutylamine → 1-cyclobutyl-4-nitro-1H-imidazole

HRID 353911
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HRID 353911 반응식
[N+]([N:4]1[CH:8]=[C:7]([N+:9]([O-:11])=[O:10])[N:6]=[CH:5]1)([O-])=O.[CH:12]1(N)[CH2:15][CH2:14][CH2:13]1>CO>[CH:12]1([N:4]2[CH:8]=[C:7]([N+:9]([O-:11])=[O:10])[N:6]=[CH:5]2)[CH2:15][CH2:14][CH2:13]1
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참가 물질

4

반응물 2

HCID 75645CyclobutylamineHCID 51694961,4-Dinitro-1H-imidazole

생성물 1

HCID 113896111-cyclobutyl-4-nitro-1H-imidazole수율 92%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

1,4-Dinitroimidazole (237 mg, 1.5 mmol, J. Phys. Chem. 1995, 99, 5009-5015) was added to a solution of cyclobutylamine (107 mg, 1.5 mmol) in methanol (10 mL) at 23° C. The reaction mixture was stirred for 16 h, then the solvent was removed in vacuo and the resulting residue was purified by silica gel chromatography (1:1 hexanes-ethyl acetate) to afford 230 mg (92% yield) of 1-cyclobutyl-4-nitro-1H-imidazole; 1H NMR (400 MHz, CDCl3) δ7.81 (s, 1H), 7.45 (s, 1H), 4.64 (m, 1H), 2.6 (m, 2H), 2.4 (m, 2H), 2.0 (m, 2H); MS (AP/Cl): 168.2 (M+H)+. Note: 1,4-Dinitroimidazole is a highly energetic, semi-stable substance and should be stored in a freezer at all times it is not in use. Thermodynamic measurements have shown that it can potentially generate enough energy at 35° C. under adiabatic conditions to violently explode. Extreme caution should be exercised at all times using this material.

후처리

  1. customthe solvent was removed in vacuo
  2. customthe resulting residue was purified by silica gel chromatography (1:1 hexanes-ethyl acetate)

출처 및 근거

ORD 기록
ord-81f9327cd9f541ff8c15345c89075ca0
출처 데이터셋
uspto-grants-2004_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06756385B2

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