Ethanol → 2-Ethoxy-5-nitropyridine

HRID 1856714노트

반응식

HRID 1856714 반응식
Cl[C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][N:3]=1.[OH-].[K+].[CH2:13]([OH:15])[CH3:14]>[Cl-].[NH4+]>[CH2:13]([O:15][C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][N:3]=1)[CH3:14]

참가 물질

5

반응물 3

HCID 702EthanolHCID 14797Potassium HydroxideHCID 783082-Chloro-5-nitropyridine

생성물 1

HCID 2958642-Ethoxy-5-nitropyridine

시약·촉매·용매 1

HCID 25517Ammonium Chloride용매

실험 절차

2-Chloro-5-nitropyridine was added to a homogeneous solution of potassium hydroxide (3.93 g, 70 mmol) in ethanol (35 mL) at ambient temperature. The reaction mixture was stirred for 1 h, then diluted with saturated aqueous ammonium chloride and cooled in an ice bath. The precipitate was collected, rinsed with water and dried to give 3.60 g of 2-ethoxy-5-nitropyridine as a beige solid.

후처리

  1. temperaturecooled in an ice bath
  2. customThe precipitate was collected
  3. washrinsed with water
  4. customdried

출처 및 근거

ORD 기록
ord-c50769b083d64a799d865218d9a973d3
출처 데이터셋
uspto-grants-2000_11
특허 번호
US06143760

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