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4,6-Dichloropyrimidine → 4-Chloro-6-(methylsulfanyl)pyrimidine

HRID 659025
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인쇄 미리보기

반응식

HRID 659025 반응식
[Cl:1][C:2]1[CH:7]=[C:6](Cl)[N:5]=[CH:4][N:3]=1.[CH3:9][S-:10].[Na+]>C1COCC1.C(OCC)(=O)C.O>[Cl:1][C:2]1[CH:7]=[C:6]([S:10][CH3:9])[N:5]=[CH:4][N:3]=1
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참가 물질

6

반응물 2

HCID 709434,6-DichloropyrimidineHCID 4378561Sodium methanethiolate

생성물 1

HCID 218130774-Chloro-6-(methylsulfanyl)pyrimidine수율 90.5%

시약·촉매·용매 3

HCID 962Water용매HCID 8028Tetrahydrofuran용매HCID 8857Ethyl Acetate용매

반응 조건

온도
60 °C

실험 절차

To a solution of 4,6-dichloro-pyrimidine (10.0 g, 67 mmol) in THF (55 ml), sodium thiomethylate (5.175 g, 74 mmol) is added under inert gas atmosphere. The reaction mixture is stirred at 60° C. overnight. After cooling down to r.t., the reaction mixture is diluted with ethyl acetate and water (100 ml each). The organic phase is removed and the aqueous phase is extracted with ethyl actetate. The combined organic phases are washed and dried, and the solvent is evaporated to give 9.74 g (90%) of a pale yellow solid (contains ca. 9% of starting material and ca. 9% of 4,6-dimethylsulfanyl-pyrimidine) which is used without any further purification.

후처리

  1. temperatureAfter cooling down to r.t.
  2. customThe organic phase is removed
  3. extractionthe aqueous phase is extracted with ethyl actetate
  4. washThe combined organic phases are washed
  5. customdried
  6. customthe solvent is evaporated

출처 및 근거

ORD 기록
ord-e94874e78eb84824a8768f65a083e4fc
출처 데이터셋
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08080552B2

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