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1-Bromo-3,5-bis(trifluoromethyl)benzene → HCID 22721470、化合物

HRID 1581452
ノート
印刷プレビュー

反応式

HRID 1581452 の反応式
[F:1][C:2]([F:16])([F:15])[C:3]1[CH:4]=[C:5]([Mg]Br)[CH:6]=[C:7]([C:9]([F:12])([F:11])[F:10])[CH:8]=1.FC(F)(F)C1C=C(Br)C=C(C(F)(F)F)C=1.Cl[C:33]1[C:42]2[C:37](=[CH:38][CH:39]=[C:40]([CH3:43])[CH:41]=2)[N:36]=[C:35]([CH3:44])[CH:34]=1.C1(P(C2C=CC=CC=2)CCCP(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>O.C1COCC1>[CH3:44][C:35]1[CH:34]=[C:33]([C:5]2[CH:4]=[C:3]([C:2]([F:16])([F:15])[F:1])[CH:8]=[C:7]([C:9]([F:12])([F:11])[F:10])[CH:6]=2)[C:42]2[C:37](=[CH:38][CH:39]=[C:40]([CH3:43])[CH:41]=2)[N:36]=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 676021-Bromo-3,5-bis(trifluoromethyl)benzeneHCID 812191,3-Bis(diphenylphosphino)propaneHCID 2342754-Chloro-2,6-dimethylquinolineHCID 178506227HCID 178506227、化合物

生成物 1

HCID 22721470HCID 22721470、化合物

試薬・触媒・溶媒 2

HCID 962Water
溶媒
HCID 8028Tetrahydrofuran溶媒

実験手順

First, 3,5-bis(trifluoromethyl)phenylmagnesium bromide prepared from Mg and 3,5-bis(trifluoromethyl)bromobenzene was dropped into a THF solution of 4-chloro-2,6-dimethylquinoline (1 g) andNi(dpp)Cl2 (dpp: 1,3-bis(diphenylphosphino)propane) (0.1 g). Reactions were allowed to take place for 24 hours at room temperature. Water was added to the reaction solution and the organic layer was extracted using CHCl3. The solvent was removed under reduced pressure and the residue was purified through column chromatography to obtain 2,6-dimethyl-4-[3,5-bis(trifluoromethyl)phenyl]quinoline (0.5 g).

後処理

  1. customfor 24 hours
  2. customat room temperature
  3. extractionthe organic layer was extracted
  4. customThe solvent was removed under reduced pressure
  5. customthe residue was purified through column chromatography

出典と根拠

ORDレコード
ord-f8702716f42b4b848dc31dd008987cff
出典データセット
uspto-grants-2004_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06730418B2

反応ノート

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