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Sodium Iodide → HCID 90389349, 화합물

HRID 1526596
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HRID 1526596 반응식
[C:1]([CH2:3][O:4][C:5]1[CH:6]=[C:7]([CH3:15])[C:8]([C:11]([O:13]C)=[O:12])=[N:9][CH:10]=1)#[N:2].[I-].[Na+].Cl[Si](C)(C)C>C(#N)C>[C:1]([CH2:3][O:4][C:5]1[CH:6]=[C:7]([CH3:15])[C:8]([C:11]([OH:13])=[O:12])=[N:9][CH:10]=1)#[N:2]
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참가 물질

5

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HCID 5238Sodium IodideHCID 6397ChlorotrimethylsilaneHCID 90389417HCID 90389417, 화합물

생성물 1

HCID 90389349HCID 90389349, 화합물

시약·촉매·용매 1

HCID 6342Acetonitrile용매

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온도
70 °C

실험 절차

To a solution of methyl 5-(cyanomethoxy)-3-methylpicolinate (0.895 g, 4.34 mmol) and sodium iodide (0.354 ml, 8.68 mmol, Sigma-Aldrich Chemical Company, Inc.) in acetonitrile (4.34 ml) was added chlorotrimethylsilane (1.102 ml, 8.68 mmol, Strem Chemicals, Inc.). The reaction mixture was heated to 70° C. and allowed to stir overnight. The reaction mixture was concentrated under reduced pressure and the residue was diluted with water and extracted with EtOAc. The organic extract was washed with water, 10% sodium thio sulfate solution and dried over MgSO4. The filtrate was concentrated in vacuo to give 5-(cyanomethoxy)-3-methylpicolinic acid which was used without further purification. MS m/z=192.9 [M+H]+. Calculated for C9H8N2O3: 192.03

후처리

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. additionthe residue was diluted with water
  3. extractionextracted with EtOAc
  4. extractionThe organic extract
  5. washwas washed with water, 10% sodium thio sulfate solution
  6. dry with materialdried over MgSO4
  7. concentrationThe filtrate was concentrated in vacuo

출처 및 근거

ORD 기록
ord-4a9192eefb3b401d9dab3276e057f268
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09085576B2

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