6-Nitroveratraldehyde → HCID 178487640, 화합물
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]=1참가 물질
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
- customsynthesized
- customThe solvent was removed from the reaction solution by distillation
- additionthe water and chloroform were then added to the residue
- extractionThe aqueous layer was extracted with chloroform
- washThe organic layer was washed with saturated brine
- dry with materialwas then dried over anhydrous sodium sulfate
- customThe solvent was removed by distillation
- 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
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