2-Chloro-3-nitropyridine → 2-Methoxy-3-nitropyridine

HRID 533948

반응식

HRID 533948 반응식
[CH3:1][O-:2].[Na+].Cl[C:5]1[C:10]([N+:11]([O-:13])=[O:12])=[CH:9][CH:8]=[CH:7][N:6]=1>CO>[CH3:1][O:2][C:5]1[C:10]([N+:11]([O-:13])=[O:12])=[CH:9][CH:8]=[CH:7][N:6]=1

참가 물질

4

반응물 2

HCID 796132-Chloro-3-nitropyridineHCID 10942334Sodium Methoxide

생성물 1

HCID 2532192-Methoxy-3-nitropyridine수율 90%

시약·촉매·용매 1

HCID 887Methanol용매2회

실험 절차

A suspension of sodium methoxide (40.5 g, 0.750 mol) in 200 mL of methanol was slowly added to a solution of 2-chloro-3-nitro-pyridine (79.3 g, 0.500 mol) in 800 mL of methanol at 0° C. The reaction mixture was stirred for 4 hours and then poured into 1000 g of ice. The resulting precipitate was filtered, washed with water, and dried to give 2-methoxy-3-nitro-pyridine (70. g, 0.45 mmol, 90%) as a white solid.

후처리

  1. filtrationThe resulting precipitate was filtered
  2. washwashed with water
  3. customdried

출처 및 근거

ORD 기록
ord-b0fac9fd81e24933abb559e336aac99b
출처 데이터셋
uspto-grants-2014_10
특허 번호
US08853415B2

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