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Chlorosuccinimide → 5-[3,5-Bis(trifluoromethyl)phenyl]-3-(4-ethylphenyl)-5-trifluoromethyl-4,5-dihydroisoxazole

HRID 1880238
ノート
印刷プレビュー

反応式

HRID 1880238 の反応式
[CH2:1]([C:3]1[CH:11]=[CH:10][C:6]([CH:7]=[N:8][OH:9])=[CH:5][CH:4]=1)[CH3:2].ClN1C(=O)CCC1=O.[F:20][C:21]([F:39])([F:38])[C:22]1[CH:23]=[C:24]([C:32]([C:34]([F:37])([F:36])[F:35])=[CH2:33])[CH:25]=[C:26]([C:28]([F:31])([F:30])[F:29])[CH:27]=1.C(=O)([O-])O.[K+]>CN(C)C=O.O>[F:20][C:21]([F:38])([F:39])[C:22]1[CH:23]=[C:24]([C:32]2([C:34]([F:37])([F:36])[F:35])[O:9][N:8]=[C:7]([C:6]3[CH:10]=[CH:11][C:3]([CH2:1][CH3:2])=[CH:4][CH:5]=3)[CH2:33]2)[CH:25]=[C:26]([C:28]([F:29])([F:30])[F:31])[CH:27]=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 31398ChlorosuccinimideHCID 516893Potassium BicarbonateHCID 20638474-EthylbenzaldoximeHCID 498208821,3-Bis(trifluoromethyl)-5-(1,1,1-trifluoroprop-2-en-2-yl)benzene

生成物 1

HCID 867616915-[3,5-Bis(trifluoromethyl)phenyl]-3-(4-ethylphenyl)-5-trifluoromethyl-4,5-dihydroisoxazole

試薬・触媒・溶媒 2

HCID 962
Water
溶媒
HCID 6228Dimethylformamide溶媒

実験手順

To a solution of 1.49 g of 4-ethylbenzaldoxime in 10 mL of N,N-dimethylformamide, 1.60 g of N-chlorosuccinimide was added and the resultant mixture was stirred at room temperature for 2 hours. Next, to the reaction mixture, 3.00 g of 3,5-bis(trifluoromethyl)-1-(1-trifluoromethylethenyl)benzene and 3.00 g of potassium hydrogen carbonate were added and the stirring of the resultant reaction mixture was continued at room temperature further for 14 hours. After the completion of the reaction, 10 mL of water was added to the reaction mixture and the resultant reaction mixture was extracted with ethyl acetate (50 mL×1). The organic phase was washed with 20 mL of water and then dehydrated and dried over saturated saline and anhydrous sodium sulfate in this order, and the solvent was distilled off under reduced pressure. To the resultant residue, hexane was added and a deposited crystal was filtered off to obtain 3.00 g of the objective substance as a white crystal.

後処理

  1. customreaction mixture
  2. additionwas added to the reaction mixture
  3. customthe resultant reaction mixture
  4. extractionwas extracted with ethyl acetate (50 mL×1)
  5. washThe organic phase was washed with 20 mL of water
  6. dry with materialdried over saturated saline and anhydrous sodium sulfate in this order
  7. distillationthe solvent was distilled off under reduced pressure
  8. additionTo the resultant residue, hexane was added
  9. filtrationa deposited crystal was filtered off
  10. customto obtain 3.00 g of the objective substance as a white crystal

出典と根拠

ORDレコード
ord-69471006fc5d4f5aa872d9264a881c9f
出典データセット
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08318757B2

反応ノート

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