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Sodium Methoxide → 4-chloro-5-methoxy-2-methoxymethyl-2H-pyridazin-3-one

HRID 2042654
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HRID 2042654 반응식
[Cl:1][C:2]1[C:3](=[O:12])[N:4]([CH2:9][O:10][CH3:11])[N:5]=[CH:6][C:7]=1Cl.[CH3:13][O-:14].[Na+]>CO>[Cl:1][C:2]1[C:3](=[O:12])[N:4]([CH2:9][O:10][CH3:11])[N:5]=[CH:6][C:7]=1[O:14][CH3:13]
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참가 물질

4

반응물 2

HCID 10942334Sodium MethoxideHCID 123518344,5-dichloro-2-methoxymethyl-2H-pyridazin-3-one

생성물 1

HCID 105843524-chloro-5-methoxy-2-methoxymethyl-2H-pyridazin-3-one수율 98.2%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a stirred solution of 4,5-dichloro-2-methoxymethyl-2H-pyridazin-3one (500 mg, 2.39 mmol) in methanol (12 mL) at room temperature was added sodium methoxide (258 mg, 4.78 mmol). After stirred for 2 h, the reaction was concentrated. To this residue was added water (20 mL), then extracted with CH2Cl2 (2×50 mL). The combined organic layer was dried (Na2SO4) and concentrated to give 480 mg (98%) 4-chloro-5-methoxy-2-methoxymethyl-2H-pyridazin-3-one.

후처리

  1. concentrationthe reaction was concentrated
  2. additionTo this residue was added water (20 mL)
  3. extractionextracted with CH2Cl2 (2×50 mL)
  4. dry with materialThe combined organic layer was dried (Na2SO4)
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-f97112d674c34f8b892dd68a6698f4e6
출처 데이터셋
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08586588B2

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