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

HRID 2216052
ノート
印刷プレビュー

反応式

HRID 2216052 の反応式
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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

HCID 218864724-Bromo-3-methyl-5-nitroaniline収率 112.8%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

(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).

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  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

出典と根拠

ORDレコード
ord-bbcb2cd734e446098911be32e8cbf4b8
出典データセット
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07109354B2

反応ノート

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