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Sodium ethoxide → 2-Ethoxy-6-methyl-5-nitronicotinonitrile

HRID 2407835
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HRID 2407835 반응식
Cl[C:2]1[N:9]=[C:8]([CH3:10])[C:7]([N+:11]([O-:13])=[O:12])=[CH:6][C:3]=1[C:4]#[N:5].[O-:14][CH2:15][CH3:16].[Na+]>C(O)C.O.C(OCC)(=O)C>[CH2:15]([O:14][C:2]1[N:9]=[C:8]([CH3:10])[C:7]([N+:11]([O-:13])=[O:12])=[CH:6][C:3]=1[C:4]#[N:5])[CH3:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 2

HCID 2723922Sodium ethoxideHCID 132403822-Chloro-6-methyl-5-nitronicotinonitrile

생성물 1

HCID 585042232-Ethoxy-6-methyl-5-nitronicotinonitrile

시약·촉매·용매 3

HCID 702Ethanol용매2회HCID 962Water용매2회HCID 8857Ethyl Acetate용매

실험 절차

To a stirred solution of the compound prepared in Example 443 (2.04 g) in ethanol (50 mL) at ambient temperature was added a 21% solution of sodium ethoxide in denatured ethanol (4.24 mL). The reaction mixture immediately turned dark purple and was stirred at ambient temperature for 2.5 hours, then diluted with water (250 mL), and the resulting mixture was stirred at ambient temperature for 3 days. The mixture was poured into a separatory funnel and diluted with water (250 mL) and ethyl acetate (500 mL). The organic layer was dried over sodium sulfate and concentrated to give about 9 g of a dark semisolid. This material was partitioned between dichloromethane (200 mL) and water (100 mL). The organic layer was dried over sodium sulfate and concentrated. The residue was purified by chromatography on silica gel, eluting with 4/1 hexanes/ethyl acetate, to provide the title compound (0.87 g) with the following physical data.

후처리

  1. stirringthe resulting mixture was stirred at ambient temperature for 3 days
  2. additionThe mixture was poured into a separatory funnel
  3. dry with materialThe organic layer was dried over sodium sulfate
  4. concentrationconcentrated

출처 및 근거

ORD 기록
ord-f22ba06ab9174243ad526ef6fa679de8
출처 데이터셋
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08809538B2

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