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Diisopropyl Ether → 1,2-Dichloro-3-(trifluoromethyl)-5-[1-(trifluoromethyl)ethenyl]benzene

HRID 1880258
ノート
印刷プレビュー

反応式

HRID 1880258 の反応式
Br[C:2]1[CH:3]=[C:4]([Cl:13])[C:5]([Cl:12])=[C:6]([C:8]([F:11])([F:10])[F:9])[CH:7]=1.C(OC(C)C)(C)C.COB(OC)OC.Br[C:29]([C:31]([F:34])([F:33])[F:32])=[CH2:30].C(=O)([O-])[O-].[K+].[K+]>CCCCCC.CCCCCC.C([Li])CCC.O1CCCC1.[Pd].C(C1C=CC=C(C(C)C)C=1N1C=CN(C2C(C(C)C)=CC=CC=2C(C)C)C1=C1CC(=O)C2C(=CC=CC=2)C1=O)(C)C.C(OCC)(=O)C.O>[Cl:13][C:4]1[CH:3]=[C:2]([C:29]([C:31]([F:34])([F:33])[F:32])=[CH2:30])[CH:7]=[C:6]([C:8]([F:11])([F:10])[F:9])[C:5]=1[Cl:12]
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

12

反応物 5

HCID 7914Diisopropyl EtherHCID 8470Trimethyl borateHCID 11430Potassium CarbonateHCID 2726961-Propene, 2-bromo-3,3,3-trifluoro-HCID 250672915-Bromo-1,2-dichloro-3-(trifluoromethyl)benzene

生成物 1

HCID 866433841,2-Dichloro-3-(trifluoromethyl)-5-[1-(trifluoromethyl)ethenyl]benzene

試薬・触媒・溶媒 6

HCID 866497721,3-Bis(2,6-diisopropylphenyl) imidazole-2-ylidene(1,4-naphthoquinone) palladium (0)触媒HCID 962Water溶媒HCID 8028Tetrahydrofuran溶媒HCID 8058Hexane溶媒HCID 8857Ethyl Acetate溶媒HCID 178418244HCID 178418244、化合物溶媒

反応条件

温度
-10 °C

実験手順

In a nitrogen atmosphere, to a solution of 26.2 g of 5-bromo-2,3-dichlorobenzotrifluoride and 9.1 g of diisopropyl ether in 250 mL of hexane, 57.5 mL of an n-butyl lithium hexane solution (1.55 M) was gradually dropped while stirring the solution at −10° C. After the completion of the dropping, the resultant mixture was stirred at the same temperature for 30 minutes. Next, into the reaction mixture, a solution of 9.26 g of trimethoxyborane in 30 mL of tetrahydrofuran was dropped and the resultant mixture was continuously stirred at room temperature further for 10 minutes. To this reaction mixture, 150 mL of water, 23.4 g of 2-bromo-3,3,3-trifluoropropene, 36.9 g of potassium carbonate and 0.131 g of 1,3-bis(2,6-diisopropylphenyl)imidazole-2-ylidene(1,4-naphthoquinone) palladium (0) dimer were added and the resultant mixture was stirred at 60° C. for 4 hours. After the completion of the reaction, the reaction mixture was left to be cooled down to room temperature, and 50 mL of ice water and 75 mL of ethyl acetate were added to the reaction mixture, followed by separating off the insoluble substance and by cleaning the insoluble substance with 75 mL of ethyl acetate. The organic phase of the filtrate was separated off and the resultant organic phase was washed with water and then dehydrated and dried over saturated saline and anhydrous sodium sulfate in this order. The solvent was distilled off under reduced pressure. The resultant residue was purified by silica gel column chromatography eluting with hexane to obtain 21.8 g of the objective substance as a colorless oily substance.

後処理

  1. customAfter the completion of the reaction
  2. waitthe reaction mixture was left
  3. temperatureto be cooled down to room temperature
  4. customby separating off the insoluble substance
  5. customThe organic phase of the filtrate was separated off
  6. washthe resultant organic phase was washed with water
  7. dry with materialdried over saturated saline and anhydrous sodium sulfate in this order
  8. distillationThe solvent was distilled off under reduced pressure
  9. customThe resultant residue was purified by silica gel column chromatography
  10. washeluting with hexane
  11. customto obtain 21.8 g of the objective substance as a colorless oily substance

出典と根拠

ORDレコード
ord-0dbe75bce2ca4d1da0c2c4062977bee0
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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