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Cyclopentanone → N-cyclopentyl-3,4,5-trifluoroaniline

HRID 1094162
ノート
印刷プレビュー

反応式

HRID 1094162 の反応式
C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].[F:15][C:16]1[CH:17]=[C:18]([CH:20]=[C:21]([F:24])[C:22]=1[F:23])[NH2:19].[C:25]1(=O)[CH2:29][CH2:28][CH2:27][CH2:26]1.C(=O)([O-])O.[Na+]>ClC(Cl)C.C(O)(=O)C>[CH:25]1([NH:19][C:18]2[CH:17]=[C:16]([F:15])[C:22]([F:23])=[C:21]([F:24])[CH:20]=2)[CH2:29][CH2:28][CH2:27][CH2:26]1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 8452CyclopentanoneHCID 516892Sodium BicarbonateHCID 27249913,4,5-TrifluoroanilineHCID 5049666Sodium triacetoxyborohydride

生成物 1

HCID 57811554N-cyclopentyl-3,4,5-trifluoroaniline

試薬・触媒・溶媒 2

HCID 176Acetic Acid溶媒
HCID 6365
1,1-Dichloroethane
溶媒

実験手順

Under ice-cooling, 11.5 g of sodium triacetoxyborohydride was added in small portions to a solution of 4.0 g of 3,4,5-trifluoroaniline and 3.6 ml cyclopentanone in 150 ml dichloroethane and 3.1 ml acetic acid, and, after rising to room temperature, stirred for 3.5 hours. Aqueous saturated sodium hydrogen carbonate was added thereto, followed by extraction with chloroform and subsequent drying over anhydrous sodium sulfate. After filtration, the solvent was evaporated under a reduced pressure, and the resulting residue was purified by silica gel column chromatography to obtain 5.4 g of N-cyclopentyl-3,4,5-trifluoroaniline.

後処理

  1. temperatureUnder ice-cooling
  2. customafter rising to room temperature
  3. extractionfollowed by extraction with chloroform
  4. dry with materialsubsequent drying over anhydrous sodium sulfate
  5. filtrationAfter filtration
  6. customthe solvent was evaporated under a reduced pressure
  7. customthe resulting residue was purified by silica gel column chromatography

出典と根拠

ORDレコード
ord-d8e83f1e36ee43dfbb921b611b931ba6
出典データセット
uspto-grants-2012_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08133882B2

反応ノート

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