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Ammonium Chloride → 3-(Trifluoromethoxy)pyridin-2-amine

HRID 2203652
ノート
印刷プレビュー

反応式

HRID 2203652 の反応式
[N+:1]([C:4]1[C:9]([O:10][C:11]([F:14])([F:13])[F:12])=[CH:8][CH:7]=[CH:6][N:5]=1)([O-])=O.[Cl-].[NH4+]>C(O)C.[Fe]>[F:14][C:11]([F:12])([F:13])[O:10][C:9]1[C:4]([NH2:1])=[N:5][CH:6]=[CH:7][CH:8]=1
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 2

HCID 25517Ammonium ChlorideHCID 19034689HCID 19034689、化合物

生成物 1

HCID 498711863-(Trifluoromethoxy)pyridin-2-amine

試薬・触媒・溶媒 2

HCID 23925Iron触媒HCID 702Ethanol溶媒

反応条件

温度
70 °C

実験手順

To a stirred solution of 2-nitro-3-(trifluoromethoxy)pyridine (370 mg, 1.78 mmol) in ethanol (5 mL) were added aqueous ammonium chloride (951 mg, 17.78 mmol, in 10 mL of water) and iron powder (993 mg, 17.78 mmol). The reaction mixture was heated to 70° C. for 2 h. After cooling down the reaction mixture was filtered and the solid was washed with ethyl acetate. The mother liquid was concentrated to dryness in vacuo. The residue was diluted with water and extracted with ethyl acetate (3×15 mL). The combined organic layers were dried over anhydrous sodium sulfate and concentrated to dryness in vacuo. The residue was used in next step directly without further purification (250 mg, 79%): 1H NMR (400 MHz, DMSO-d6) δ 7.93-7.91 (m, 1H), 7.48-7.46 (m, 1H), 6.59-6.56 (m, 1H), 6.35 (brs, 2H).

後処理

  1. temperatureAfter cooling down the reaction mixture
  2. filtrationwas filtered
  3. washthe solid was washed with ethyl acetate
  4. concentrationThe mother liquid was concentrated to dryness in vacuo
  5. additionThe residue was diluted with water
  6. extractionextracted with ethyl acetate (3×15 mL)
  7. dry with materialThe combined organic layers were dried over anhydrous sodium sulfate
  8. concentrationconcentrated to dryness in vacuo
  9. customThe residue was used in next step directly without further purification (250 mg, 79%)

出典と根拠

ORDレコード
ord-96f4d3aae38045bf9bb9b737d394ae85
出典データセット
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09365583B2

反応ノート

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