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Hydrochloric Acid → HCID 68831193, 화합물

HRID 747709
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HRID 747709 반응식
Cl[CH2:2][CH2:3][CH2:4][CH2:5][C:6]([C:8]1[CH:15]=[CH:14][C:11]([C:12]#[N:13])=[CH:10][CH:9]=1)=[O:7].C(=O)([O-])[O-].[K+].[K+].[I-].[K+].[OH:24][C:25]1[CH:26]=[C:27]([CH:30]=[CH:31][CH:32]=1)[C:28]#[N:29].Cl>CN(C)C=O>[C:12]([C:11]1[CH:14]=[CH:15][C:8]([C:6](=[O:7])[CH2:5][CH2:4][CH2:3][CH2:2][O:24][C:25]2[CH:26]=[C:27]([CH:30]=[CH:31][CH:32]=2)[C:28]#[N:29])=[CH:9][CH:10]=1)#[N:13]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 5

HCID 313Hydrochloric AcidHCID 4875Potassium IodideHCID 11430Potassium CarbonateHCID 133943-CyanophenolHCID 177891304-(5-Chloropentanoyl)benzonitrile

생성물 1

HCID 68831193HCID 68831193, 화합물

시약·촉매·용매 1

HCID 6228
Dimethylformamide
용매

반응 조건

온도
70 °C

실험 절차

53 mg (0.24 mmol) of 4-(5-chloro-1-oxopentyl)benzonitrile was dissolved in 2 ml of dimethylformamide. 33 mg (0.24 mmol) of potassium carbonate, 40 mg of potassium iodide and 29 mg (0.24 mmol) of 3-hydroxybenzonitrile were added to the solution, and they were stirred at 70° C. overnight. 1 N Hydrochloric acid was added to the reaction mixture. After the extraction with ethyl acetate, the extract was washed with 1 N aqueous sodium hydroxide solution and saturated aqueous common salt solution, and then dried over powdery magnesium sulfate. The solvent was evaporated, and the residue was purified by the silica gel chromatography to obtain the title compound.

후처리

  1. extractionAfter the extraction with ethyl acetate
  2. washthe extract was washed with 1 N aqueous sodium hydroxide solution and saturated aqueous common salt solution
  3. dry with materialdried over powdery magnesium sulfate
  4. customThe solvent was evaporated
  5. customthe residue was purified by the silica gel chromatography

출처 및 근거

ORD 기록
ord-2b5e7c2bcbae490aa06a6c5fe28e967c
출처 데이터셋
uspto-grants-2008_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07396844B1

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