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Trimethyl borate → HCID 86654468、化合物

HRID 878855
ノート
印刷プレビュー

反応式

HRID 878855 の反応式
Br[C:2]1[CH:3]=[C:4]([C:9]([F:12])([F:11])[F:10])[CH:5]=[C:6]([Cl:8])[CH:7]=1.COB(OC)OC.Br[C:21]([C:23]([F:26])([F:25])[F:24])=[CH2:22].C(=O)([O-])[O-].[K+].[K+]>CCCCCC.C([Li])CCC.O1CCCC1.O.C(OC)(C)(C)C>[Cl:8][C:6]1[CH:7]=[C:2]([C:21]([C:23]([F:26])([F:25])[F:24])=[CH2:22])[CH:3]=[C:4]([C:9]([F:12])([F:11])[F:10])[CH:5]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

10

反応物 4

HCID 8470Trimethyl borateHCID 11430Potassium CarbonateHCID 2726961-Propene, 2-bromo-3,3,3-trifluoro-HCID 202698551-Bromo-3-chloro-5-(trifluoromethyl)benzene

生成物 1

HCID 86654468HCID 86654468、化合物

試薬・触媒・溶媒 5

HCID 962Water溶媒
HCID 8028
Tetrahydrofuran
溶媒
HCID 8058Hexane溶媒
HCID 15413tert-Butyl methyl ether溶媒
HCID 178418339Butyllithium溶媒

実験手順

In a solution of 2.60 g of 3-bromo-5-chlorobenzotrifluoride and 1.2 mL of tert-butylmethyl ether in 25 mL of hexane, 6.38 mL of n-butyl lithium (1.6M hexane solution) was added dropwise at −10° C. with stirring, and stirred at the same temperature for 30 minutes. Then, a solution of 1.09 g of trimethoxyborane in 10 mL of tetrahydrofuran was added dropwise. After the completion of the addition dropwise, it was stirred at the same temperature further for 10 minutes and then the temperature was raised to room temperature. Then, in the reaction mixture, 2.60 g of 2-bromo-3,3,3-trifluoropropene, 2.76 g of potassium carbonate, 15 mL of water and 0.0065 g of 1,3-bis(2,6-diisopropylphenyl)imidazole-2-ilidene (1,4-naphthoquinone) palladium (0) dimmer were added, and stirred under nitrogen atmosphere at 60° C. for 6 hours. After the completion of the reaction, the reaction mixture was left and cooled to room temperature, insoluble material was filtered off, and the organic phase was collected and the aqueous phase was extracted with 30 mL of ethyl acetate twice.

後処理

  1. stirringstirred at the same temperature for 30 minutes
  2. additionAfter the completion of the addition dropwise
  3. stirringit was stirred at the same temperature further for 10 minutes
  4. stirringstirred under nitrogen atmosphere at 60° C. for 6 hours
  5. customAfter the completion of the reaction
  6. waitthe reaction mixture was left
  7. temperaturecooled to room temperature
  8. filtrationinsoluble material was filtered off
  9. customthe organic phase was collected
  10. extractionthe aqueous phase was extracted with 30 mL of ethyl acetate twice

出典と根拠

ORDレコード
ord-d9efd0649ad740fbaa4cf14486739830
出典データセット
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08987464B2

反応ノート

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