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Cesium fluoride → HCID 67122548、化合物

HRID 706365
ノート
印刷プレビュー

反応式

HRID 706365 の反応式
[CH3:1][O:2][C:3](=[O:13])[C:4]#[C:5][C:6]1[CH:11]=[CH:10][C:9]([Cl:12])=[CH:8][CH:7]=1.[F-:14].[Cs+].F.[K]>CN(C)C=O.O.C(OCC)(=O)C>[CH3:1][O:2][C:3](=[O:13])/[CH:4]=[C:5](/[C:6]1[CH:11]=[CH:10][C:9]([Cl:12])=[CH:8][CH:7]=1)\[F:14]
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

7

反応物 3

HCID 25953Cesium fluorideHCID 825800(4-chloro-phenyl)-propynoic acid methyl esterHCID 53443437Potassium fluoride, 99%, spray-dried

生成物 1

HCID 67122548HCID 67122548、化合物収率 20%

試薬・触媒・溶媒 3

HCID 962Water溶媒HCID 6228Dimethylformamide溶媒
HCID 8857Ethyl Acetate溶媒

反応条件

温度
80 °C

実験手順

To a solution of (4-chloro-phenyl)-propynoic acid methyl ester (5.36 g) in dimethylformamide (60 ml) was added cesium fluoride (11.4 g) and potassium hydrogen fluoride (2.73 g) in water (5.4 ml) and the mixture was stirred at 80° C. for 8 h. The reaction mixture was cooled to room temperature, diluted with ethyl acetate (50 ml), the organic phase washed with water (3×50 ml) and brine (3×20 ml), dried over sodium sulfate and concentrated in vacuo. The residue was purified by column chromatography (SiO2, ethyl acetate:cyclohexan 1:9) to give 1.06 g of the desired product (20%) which was characterized by its mass and NMR spectra.

後処理

  1. temperatureThe reaction mixture was cooled to room temperature
  2. washthe organic phase washed with water (3×50 ml) and brine (3×20 ml)
  3. dry with materialdried over sodium sulfate
  4. concentrationconcentrated in vacuo
  5. customThe residue was purified by column chromatography (SiO2, ethyl acetate:cyclohexan 1:9)

出典と根拠

ORDレコード
ord-9491661fbd6c44d0ab2bbcb1a8734e9a
出典データセット
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09174987B2

反応ノート

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