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Dimethylformamide → 2-(3-Cyano-4-nitrophenyl)-2-methyl-1,3-dioxolane

HRID 1087190
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HRID 1087190 반응식
Cl[C:2]1[CH:3]=[C:4]([C:11]2([CH3:16])[O:15][CH2:14][CH2:13][O:12]2)[CH:5]=[CH:6][C:7]=1[N+:8]([O-:10])=[O:9].C(=O)(O)[O-].[Na+].C(OCC)(=O)C.[CH3:28][N:29](C)C=O>>[C:28]([C:2]1[CH:3]=[C:4]([C:11]2([CH3:16])[O:15][CH2:14][CH2:13][O:12]2)[CH:5]=[CH:6][C:7]=1[N+:8]([O-:10])=[O:9])#[N:29]
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참가 물질

5

반응물 4

HCID 6228DimethylformamideHCID 8857Ethyl AcetateHCID 516892Sodium BicarbonateHCID 100374432-(3-Chloro-4-nitrophenyl)-2-methyl-1,3-dioxolane

생성물 1

HCID 100142372-(3-Cyano-4-nitrophenyl)-2-methyl-1,3-dioxolane

실험 절차

A mixture of 2-(3-chloro-4-nitrophenyl)-2-methyl-1,3-dioxolane (9.8 g) and cuprous cyanide (4.0 g) in N,N-dimethylformamide (20 ml) was stirred and refluxed for 11 hours. An aqueous solution of sodium bicarbonate (200 ml) and ethyl acetate (100 ml) were added to the reaction mixture. The mixture was stirred and filtered. The filtrate was separated and the organic layer was dried and evaporated. The oily residue was purified by column chromatography on silica gel (200 g) eluting with a mixture of toluene and ethyl acetate (20:1) to give yellow plates of 2-(3-cyano-4-nitrophenyl)-2-methyl-1,3-dioxolane (4.6 g).

후처리

  1. temperaturerefluxed for 11 hours
  2. stirringThe mixture was stirred
  3. filtrationfiltered
  4. customThe filtrate was separated
  5. customthe organic layer was dried
  6. customevaporated
  7. customThe oily residue was purified by column chromatography on silica gel (200 g)
  8. washeluting with a mixture of toluene and ethyl acetate (20:1)

출처 및 근거

ORD 기록
ord-0f93b2f3423b45ebbe194eaa33773e46
출처 데이터셋
uspto-grants-1991_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05034417

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