Trifluoroacetic acid → 3-Dipropylamino-5-nitrochroman

HRID 1684067

反応式

HRID 1684067 の反応式
[CH2:1]([N:4]([CH2:16][CH2:17][CH3:18])[CH:5]1[CH2:14][C:13]2[C:8](=[CH:9][CH:10]=[CH:11][C:12]=2N)[O:7][CH2:6]1)[CH2:2][CH3:3].FC(F)(F)C(O)=O.[N:26]([O-:28])=[O:27].[Na+].C(=O)([O-])[O-].[Ca+2]>O.S([O-])([O-])(=O)=O.[Cu+2].[Cu-]=O>[CH2:16]([N:4]([CH2:1][CH2:2][CH3:3])[CH:5]1[CH2:14][C:13]2[C:8](=[CH:9][CH:10]=[CH:11][C:12]=2[N+:26]([O-:28])=[O:27])[O:7][CH2:6]1)[CH2:17][CH3:18]

参加物

8

実験手順

3-Dipropylamino-5-aminochroman (Example 14; 0.050 g, 0.20 mmol) was dissolved in a mixture of trifluoracetic acid (0.080 ml, 1.0 mmol) in water (5 ml). The clear solution was cooled to 0°-4° C. Sodium nitrite (0.017 g, 2.5 mmol) in water (1.0 ml), was added dropwise with good stirring. The solution was stirred for 15 minutes and neutralized with calcium carbonate. A solution of sodium nitrite (0.50 g, 7.2 mmol) in water (1.0 ml) was added followed by a mixture of copper sulfate (0.10 g, 0.62 mmol) and copper (1) oxide in water (1.0 ml). The solution was stirred at 0° C. for 20 minutes and then at ambient temperature for 2 hours. The solution was extracted with diethyl ether. The organic phase was dried with sodium sulfate and evaporated to dryness. The residue was purified by flash chromatography on silica gel by elution with ethyl acetate/hexane 1:9 to give the title compound. Mp 150°-151° C. (hydrochloride).

後処理

  1. temperatureThe clear solution was cooled to 0°-4° C
  2. stirringThe solution was stirred at 0° C. for 20 minutes
  3. waitat ambient temperature for 2 hours
  4. extractionThe solution was extracted with diethyl ether
  5. dry with materialThe organic phase was dried with sodium sulfate
  6. customevaporated to dryness
  7. customThe residue was purified by flash chromatography on silica gel by elution with ethyl acetate/hexane 1:9

出典と根拠

ORDレコード
ord-fd4a0eeed4924ace92a8875ae4f6c36d
出典データセット
uspto-grants-1997_06
特許番号
US05639772

関連ノート

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