Ethanolamine → 2-[(2-Bromo-6-nitrophenyl)amino]ethanol

HRID 1991183노트

반응식

HRID 1991183 반응식
[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([N+:8]([O-:10])=[O:9])[C:3]=1Cl.[CH2:12]([CH2:14][NH2:15])[OH:13]>C(O)C>[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([N+:8]([O-:10])=[O:9])[C:3]=1[NH:15][CH2:14][CH2:12][OH:13]

참가 물질

4

실험 절차

A solution of 1-bromo-2-chloro-3-nitrobenzene (0.34 g, 1.4 mmol) and ethanolamine (0.22 mL, 3.5 mmol) in dry ethanol (3.8 mL) was irradiated in a microwave oven at 135° C. for 180 min. After the reaction mixture was concentrated under reduced pressure. The residue was dissolved in ethyl acetate, the organic phase was washed with potassium bisulfate (0.1 M), water and brine, dried over Na2SO4 and concentrated. Purification was performed using flash chromatography on a silica column and 25% ethyl acetate in heptane as an eluent to yield 2-[(2-bromo-6-nitrophenyl)amino]ethanol as red oil, 0.24 g (65%). 1H NMR (400 MHz, DMSO-D6) δ ppm 3.13 (q, J=5.2 Hz, 2H) 3.51 (q, J=5.1 Hz, 2H) 4.87 (t, J=5.1 Hz, 1H) 6.18 (t, J=5.1 Hz, 1H) 6.80 (t, J=8.1 Hz, 1H) 7.84 (dd, J=7.8, 3.3 Hz, 2H).

후처리

  1. concentrationAfter the reaction mixture was concentrated under reduced pressure
  2. dissolutionThe residue was dissolved in ethyl acetate
  3. washthe organic phase was washed with potassium bisulfate (0.1 M), water and brine
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated
  6. customPurification

출처 및 근거

ORD 기록
ord-5e4723329dd040d5b5e24717915fd1c3
출처 데이터셋
uspto-grants-2010_01
특허 번호
US07645784B2

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