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Cesium fluoride → HCID 67122548, 화합물

HRID 706365
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HRID 706365 반응식
[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]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

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

생성물 1

HCID 67122548HCID 67122548, 화합물수율 20%

시약·촉매·용매 3

HCID 962Water용매HCID 6228Dimethylformamide용매
HCID 8857Ethyl Acetate용매

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온도
80 °C

실험 절차

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.

후처리

  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)

출처 및 근거

ORD 기록
ord-9491661fbd6c44d0ab2bbcb1a8734e9a
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09174987B2

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