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Isopropanol → 2-Isopropoxynicotinonitrile

HRID 1819439
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인쇄 미리보기

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HRID 1819439 반응식
Cl[C:2]1[N:9]=[CH:8][CH:7]=[CH:6][C:3]=1[C:4]#[N:5].[CH3:10][CH:11]([OH:13])[CH3:12].[OH-].[K+].C1OCCOCCOCCOCCOCCOC1>C1(C)C=CC=CC=1>[CH:11]([O:13][C:2]1[N:9]=[CH:8][CH:7]=[CH:6][C:3]=1[C:4]#[N:5])([CH3:12])[CH3:10]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 3776IsopropanolHCID 14797Potassium HydroxideHCID 2855718-Crown-6HCID 810792-Chloronicotinonitrile

생성물 1

HCID 126045132-Isopropoxynicotinonitrile수율 94.2%

시약·촉매·용매 1

HCID 1140Toluene용매

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온도
60 °C

실험 절차

A mixture of 2-chloronicotinonitrile (1.0 g, 7.2 mmol), 2-propanol (0.87 g, 14.4 mmol), KOH (0.81 g, 14.4 mmol) and 18-crown-6 (1.8 g, 2.89 mmol) in toluene (30 mL) was stirred at 60° C. for 16 h. The reaction mixture was quenched with water and the organic phase was separated and then washed with water (×5). The organic phase was dried over Na2SO4 and concentrated to yield crude 2-isopropoxy-nicotinonitrile (1.1 g, 94%) which was used without further purification.

후처리

  1. customThe reaction mixture was quenched with water
  2. customthe organic phase was separated
  3. washwashed with water (×5)
  4. dry with materialThe organic phase was dried over Na2SO4
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-5492a231859247efa6562ff1d10fbab6
출처 데이터셋
uspto-grants-2009_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07601714B2

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