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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Water → 5-Hydroxypyridine-3-carbonitrile

HRID 334412
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인쇄 미리보기

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HRID 334412 반응식
C[O:2][C:3]1[CH:4]=[N:5][CH:6]=[C:7]([CH:10]=1)[C:8]#[N:9].Cl.N1C=CC=CC=1.O.C(=O)(O)[O-].[Na+]>C(OCC)C>[OH:2][C:3]1[CH:4]=[N:5][CH:6]=[C:7]([CH:10]=1)[C:8]#[N:9]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 516892Sodium BicarbonateHCID 10176127Pyridinium chlorideHCID 231597785-Methoxypyridine-3-carbonitrile

생성물 1

HCID 153421425-Hydroxypyridine-3-carbonitrile수율 95%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

반응 조건

온도
200 °C

실험 절차

A mixture of 1 g of 5-methoxynicotinonitrile (7.46 mmol) and 8.62 g of pyridine hydrochloride is heated at 200° C. for 2 hours. The crude reaction product is diluted in a water fraction several times with diethyl ether. The aqueous phase is basified by adding sodium bicarbonate and then extracted again with diethyl ether. The organic phase is dried and then concentrated to yield 850 mg of 5-hydroxynicotinonitrile (95%) in the form of a beige solid.

후처리

  1. customThe crude reaction product
  2. extractionextracted again with diethyl ether
  3. customThe organic phase is dried
  4. concentrationconcentrated

출처 및 근거

ORD 기록
ord-1a14881e0a124b9dbf8f7a491c553bf3
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08883821B2

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