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Cesium fluoride → HCID 20036689、化合物

HRID 1904976
ノート
印刷プレビュー

反応式

HRID 1904976 の反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([C:11]([F:14])([F:13])[F:12])[CH2:9][OH:10])=[CH:4][CH:3]=1.O([C:22]1[CH:23]=[C:24]([CH:27]=[CH:28][CH:29]=1)[CH2:25]Br)C1C=CC=CC=1.[F-].[Cs+]>COCCOCCOC>[C:2]1([C:22]2[CH:23]=[C:24]([CH:27]=[CH:28][CH:29]=2)[CH2:25][O:10][CH2:9][CH:8]([C:5]2[CH:6]=[CH:7][C:2]([F:1])=[CH:3][CH:4]=2)[C:11]([F:12])([F:13])[F:14])[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 25953Cesium fluorideHCID 945441-(Bromomethyl)-3-phenoxybenzeneHCID 20036620HCID 20036620、化合物

生成物 1

HCID 20036689HCID 20036689、化合物

試薬・触媒・溶媒 1

HCID 8150Diglyme溶媒

実験手順

Under a nitrogen atmosphere, 0.50 g of 2-(4-fluorophenyl)-3,3,3-trifluoropropanol and 0.63 g of 3-phenoxybenzyl bromide was dissolved in 15 ml of dry diethyleneglycol dimethylether. Into the solution, 1.83 g of dry cesium fluoride was added at room temperature, and the reaction solution was stirred at room temperature for 48 hours. Thereafter, the reaction solution was poured into dilute HCl-ice water and extracted twice with diethyl ether. The ether layers were combined, washed with saturated sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent was removed under a reduced pressure, and the residue was subjected to preparative thin-layer chromatography on silica gel to obtain αmg of the desired compound.

後処理

  1. extractionextracted twice with diethyl ether
  2. washwashed with saturated sodium chloride solution
  3. dry with materialdried over anhydrous magnesium sulfate
  4. customThe solvent was removed under a reduced pressure

出典と根拠

ORDレコード
ord-2555e011882e465fa4f4d72c3fc2b5e6
出典データセット
uspto-grants-1989_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04840971

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート