Allyl bromide → 2-[(2-Propenyloxy)-methyl]-5-nitrobenzenamine

HRID 225494

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HRID 225494 반응식
[NH2:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[CH:4][C:3]=1[CH2:11][OH:12].[CH3:13][C:14]([O-])(C)[CH3:15].[K+].C(Br)C=C>C1COCC1.C(OCC)(=O)C>[CH2:15]([O:12][CH2:11][C:3]1[CH:4]=[CH:5][C:6]([N+:8]([O-:10])=[O:9])=[CH:7][C:2]=1[NH2:1])[CH:14]=[CH2:13]

참가 물질

6

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온도
0 °C

실험 절차

A stirred solution of 2-amino-4-nitrobenzenemethanol (14.3 g, 85 mmol) in dry THF (350 mL) at 0° C. under an argon atmosphere, is treated dropwise over 35 min with a solution of potassium tert-butylate in THF (Fluka; 85 mL of 1.0 M). The mixture is stirred at 0° C. for 15 min and then treated dropwise over 50 min with a solution of allylbromide (7.9 mL, 94 mmol) in dry THF (80 mL) at 0° C. and then stirred at 20° C. for 90 min. The mixture is diluted with ethyl acetate (800 mL). The resulting solution is washed with saturated aqueous ammonium chloride (3×400 mL), dried (MgSO4), filtered and the solvent is evaporated off under reduced pressure to yield the crude product which is purified by column chromatography on silica gel, eluent 50% ethyl acetate in hexane, to give the title compound as a brown oil.

후처리

  1. stirringstirred at 20° C. for 90 min
  2. washThe resulting solution is washed with saturated aqueous ammonium chloride (3×400 mL)
  3. dry with materialdried (MgSO4)
  4. filtrationfiltered
  5. customthe solvent is evaporated off under reduced pressure
  6. customto yield the crude product which
  7. customis purified by column chromatography on silica gel, eluent 50% ethyl acetate in hexane

출처 및 근거

ORD 기록
ord-3368b4e0080f4501b090a6f926e165fa
출처 데이터셋
uspto-grants-2009_07
특허 번호
US07557105B2

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