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Ethanol → Methyl 3-amino-2-methyl-5-(trifluoromethyl)benzoate

HRID 1501702
ノート
印刷プレビュー

反応式

HRID 1501702 の反応式
[CH3:1][C:2]1[C:11]([N+:12]([O-])=O)=[CH:10][C:9]([C:15]([F:18])([F:17])[F:16])=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5].C(O)C.[NH4+].[Cl-]>[Fe]>[NH2:12][C:11]1[C:2]([CH3:1])=[C:3]([CH:8]=[C:9]([C:15]([F:16])([F:17])[F:18])[CH:10]=1)[C:4]([O:6][CH3:7])=[O:5]
参加物反応条件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 702EthanolHCID 25517Ammonium ChlorideHCID 68295416Methyl 2-methyl-3-nitro-5-(trifluoromethyl)benzoate

生成物 1

HCID 68295733Methyl 3-amino-2-methyl-5-(trifluoromethyl)benzoate

試薬・触媒・溶媒 1

HCID 23925Iron触媒

反応条件

温度
90 °C

実験手順

To a stirred solution of methyl 2-methyl-3-nitro-5-(trifluoromethyl)benzoate (1 equiv.) in ethanol (2 mL per 1 mmol), was added NH4Cl solution (5.1 equiv., dissolved in water. Volume of water equivalent to volume of ethanol) followed by Fe powder (8 equiv.). the resulting reaction mixture was stirred at 90° C. for 1 h. On completion, the reaction mixture was filtered and the filtrate concentrated till dryness. The resulting solid was dissolved in saturated sodium bicarbonate solution and the aqueous layer extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate and concentrated to afford solid methyl 3-amino-2-methyl-5-(trifluoromethyl)benzoate in quantitative yield.

後処理

  1. customthe resulting reaction mixture
  2. filtrationOn completion, the reaction mixture was filtered
  3. concentrationthe filtrate concentrated till dryness
  4. dissolutionThe resulting solid was dissolved in saturated sodium bicarbonate solution
  5. extractionthe aqueous layer extracted with ethyl acetate
  6. dry with materialThe combined organic layers were dried over sodium sulfate
  7. concentrationconcentrated

出典と根拠

ORDレコード
ord-c3e1b3dd693b41298c4cfac8ee131de7
出典データセット
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09206157B2

反応ノート

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