6-Nitroveratraldehyde → HCID 178487640, 화합물

HRID 251798노트

반응식

HRID 251798 반응식
[CH3:1][O:2][C:3]1[C:10]([O:11][CH3:12])=[CH:9][C:6]([CH:7]=[O:8])=[C:5]([N+:13]([O-:15])=[O:14])[CH:4]=1.[F-].[K+].C1([S:24][CH:25]([N:30]=[C:31]=S)[Si](C)(C)C)C=CC=CC=1>[Cl-].C([N+](CC)(CC)CC)C1C=CC=CC=1.C(#N)C>[CH3:1][O:2][C:3]1[C:10]([O:11][CH3:12])=[CH:9][C:6]([C:7]2[O:8][C:25]([SH:24])=[N:30][CH:31]=2)=[C:5]([N+:13]([O-:15])=[O:14])[CH:4]=1

참가 물질

6

실험 절차

4,5-Dimethoxy-2-nitrobenzaldehyde (1.52 g, 7.19 mmol), 353.0 mg (6.07 mmol) of potassium fluoride, and 134.8 mg (0.59 mmol) of benzyltriethylammonium chloride were added to a solution of 1.51 g (5.97 mmol) of phenylthio(trimethylsilyl)methyl isothiocyanate, synthesized according to a document (J. Chem. Soc., Perkin Trans 1 1984, 435.), in acetonitrile (36 ml), and the mixture was stirred at room temperature overnight. The solvent was removed from the reaction solution by distillation, and the water and chloroform were then added to the residue. The aqueous layer was extracted with chloroform. The organic layer was washed with saturated brine and was then dried over anhydrous sodium sulfate. The solvent was removed by distillation. The residue was purified by column chromatography on silica gel (n-hexane:ethyl acetate=5:1→1:1) to give 302.4 mg (yield 18%) of the title compound.

후처리

  1. customsynthesized
  2. customThe solvent was removed from the reaction solution by distillation
  3. additionthe water and chloroform were then added to the residue
  4. extractionThe aqueous layer was extracted with chloroform
  5. washThe organic layer was washed with saturated brine
  6. dry with materialwas then dried over anhydrous sodium sulfate
  7. customThe solvent was removed by distillation
  8. customThe residue was purified by column chromatography on silica gel (n-hexane:ethyl acetate=5:1→1:1)

출처 및 근거

ORD 기록
ord-28be155f82dd4f2bb9d6b853b28f3c64
출처 데이터셋
uspto-grants-2011_01
특허 번호
US07867980B2

반응 노트

불러오는 중…