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Trifluoroacetic acid → 4-Bromo-3-methyl-5-nitroaniline

HRID 2216052
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HRID 2216052 반응식
C(OC(=O)[NH:7][C:8]1[CH:13]=[C:12]([N+:14]([O-:16])=[O:15])[C:11]([Br:17])=[C:10]([CH3:18])[CH:9]=1)(C)(C)C.C(O)(C(F)(F)F)=O.[OH-].[Na+]>C(Cl)Cl>[Br:17][C:11]1[C:12]([N+:14]([O-:16])=[O:15])=[CH:13][C:8]([NH2:7])=[CH:9][C:10]=1[CH3:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6422Trifluoroacetic acidHCID 14798Sodium HydroxideHCID 69586631(4-Bromo-3-methyl-5-nitro-phenyl)-carbamic acid tert-butyl ester

생성물 1

HCID 218864724-Bromo-3-methyl-5-nitroaniline수율 112.8%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

(4-Bromo-3-methyl-5-nitro-phenyl)-carbamic acid tert-butyl ester (1000 mg, 2.9 mmol) was dissolved into DCM (10 mL). To this was added TFA (10 mL) and the reaction was stirred at RT for 1 hour. The pH was adjusted to 8 with 1 N NaOH and the solvents were removed in vacuo. The reaction mixture was dissolved into EtOAc and the layers were separated. The organic layers were dried (MgSO4) and the solvents were removed in vacuo resulting in title compound (756 mg, quantitative) as a brown oil. 1H-NMR (CDCl3): δ 8.44 (s, 1H), 8.02 (s, 1H), 7.61 (s, 1H), 3.05 (s, 3H).

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후처리

  1. customthe solvents were removed in vacuo
  2. dissolutionThe reaction mixture was dissolved into EtOAc
  3. customthe layers were separated
  4. dry with materialThe organic layers were dried (MgSO4)
  5. customthe solvents were removed in vacuo

출처 및 근거

ORD 기록
ord-bbcb2cd734e446098911be32e8cbf4b8
출처 데이터셋
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07109354B2

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