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Trimethylsilyl cyanide → 2-(3-Hydroxypropoxy)-2-(2-methylpyrimidin-5-yl)acetonitrile

HRID 512205
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HRID 512205 반응식
[O:1]1[CH2:6][CH2:5][CH2:4][O:3][CH:2]1[C:7]1[CH:8]=[N:9][C:10]([CH3:13])=[N:11][CH:12]=1.C[Si]([C:18]#[N:19])(C)C>C(Cl)Cl.[I-].[Zn+2].[I-]>[OH:1][CH2:6][CH2:5][CH2:4][O:3][CH:2]([C:7]1[CH:8]=[N:9][C:10]([CH3:13])=[N:11][CH:12]=1)[C:18]#[N:19]
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참가 물질

5

반응물 2

HCID 82115Trimethylsilyl cyanideHCID 867162345-(1,3-Dioxan-2-yl)-2-methylpyrimidine

생성물 1

HCID 867162352-(3-Hydroxypropoxy)-2-(2-methylpyrimidin-5-yl)acetonitrile

시약·촉매·용매 2

HCID 9883512zinc(II)iodide촉매HCID 6344Dichloromethane용매

실험 절차

To an ice-cold solution of 5-(1,3-dioxan-2-yl)-2-methylpyrimidine (140 mg, 0.78 mmol) in DCM (5.0 ml) was added zinc iodide (124 mg, 0.39 mmol). Trimethylsilyl cyanide (116 mg, 0.155 ml, 1.17 mmol) was added dropwise over a period of 10 minutes. Cooling was removed and the reaction was stirred for 40 hours at room temperature. The mixture was poured into H2O (20 mL) and extracted with DCM (3×20 mL), the combined org. phases were washed with brine, dried over MgSO4 and concetrated in vacuo. The crude product was used for next step without further purification.

후처리

  1. temperatureCooling
  2. customwas removed
  3. additionThe mixture was poured into H2O (20 mL)
  4. extractionextracted with DCM (3×20 mL)
  5. washphases were washed with brine
  6. dry with materialdried over MgSO4
  7. customThe crude product was used for next step without further purification

출처 및 근거

ORD 기록
ord-477fabcd63da4690bd2f007b21273973
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09102591B2

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