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2,4,5-Trichloropyrimidine → 2,5-Dichloro-4-methoxypyrimidine

HRID 1028123
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HRID 1028123 반응식
[CH3:1][O-:2].[Na+].[Cl:4][C:5]1[N:10]=[C:9](Cl)[C:8]([Cl:12])=[CH:7][N:6]=1>CO>[Cl:4][C:5]1[N:10]=[C:9]([O:2][CH3:1])[C:8]([Cl:12])=[CH:7][N:6]=1
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참가 물질

4

반응물 2

HCID 2372592,4,5-TrichloropyrimidineHCID 10942334Sodium Methoxide

생성물 1

HCID 497617462,5-Dichloro-4-methoxypyrimidine수율 57.1%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

Sodium methoxide (295 mg, 5.45 mmol) was taken up in methanol (13.6 ml) and 2,4,5-trichloropyrimidine (500 mg, 2.73 mmol) was added. The mixture was stirred at room temperature overnight. The resulting mixture was concentrated under reduced pressure. The resulting residue was diluted with diethyl ether, washed with 1:1 water:saturated aqueous ammonium chloride. The organic layer was dried over magnesium sulfate, filtered, and concentrated under reduced pressure. Purification by Combiflash (0-10% diethyl ether/hexanes) afforded 280 mg (1.56 mmol, 57%) of 2,5-dichloro-4-methoxypyrimidine as a white solid.

후처리

  1. concentrationThe resulting mixture was concentrated under reduced pressure
  2. additionThe resulting residue was diluted with diethyl ether
  3. washwashed with 1:1 water
  4. dry with materialThe organic layer was dried over magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure
  7. customPurification by Combiflash (0-10% diethyl ether/hexanes)

출처 및 근거

ORD 기록
ord-e5b541d08cd24fa29b3bf6d785751341
출처 데이터셋
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08735417B2

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