Potassium Carbonate → Methyl 3-(4-fluoro-2-nitrophenylamino)-2-methylpropanoate

HRID 1485434노트

반응식

HRID 1485434 반응식
F[C:2]1[CH:7]=[CH:6][C:5]([F:8])=[CH:4][C:3]=1[N+:9]([O-:11])=[O:10].[NH2:12][CH2:13][CH:14]([CH3:19])[C:15]([O:17][CH3:18])=[O:16].C(=O)([O-])[O-].[K+].[K+]>O1CCCC1>[F:8][C:5]1[CH:6]=[CH:7][C:2]([NH:12][CH2:13][CH:14]([CH3:19])[C:15]([O:17][CH3:18])=[O:16])=[C:3]([N+:9]([O-:11])=[O:10])[CH:4]=1

참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 677672,5-DifluoronitrobenzeneHCID 10486829Methyl 3-amino-2-methylpropanoate

생성물 1

HCID 70978244Methyl 3-(4-fluoro-2-nitrophenylamino)-2-methylpropanoate수율 61%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 1,4-difluoro-2-nitrobenzene (14.3 g, 90 mmol) in tetrahydrofuran (250 mL) was added methyl 3-amino-2-methylpropanoate (10.5 g, 90 mmol) and potassium carbonate (24.8 g, 180 mmol). The reaction mixture was heated to reflux and stirred for 15 hours. Then the mixture was concentrated in vacuo, and the residue was dissolved in water (250 mL), extracted with ethyl acetate (100 mL*3). The combined organic layers was separated, dried over anhydrous sodium sulfate, and concentrated to give a residue. The residue was purified by column chromatography (silica gel, petroleum ether/ethyl acetate=5:1) to afford methyl 3-(4-fluoro-2-nitrophenylamino)-2-methylpropanoate as a red solid (14.0 g, 61%).

후처리

  1. temperatureThe reaction mixture was heated
  2. temperatureto reflux
  3. concentrationThen the mixture was concentrated in vacuo
  4. dissolutionthe residue was dissolved in water (250 mL)
  5. extractionextracted with ethyl acetate (100 mL*3)
  6. customThe combined organic layers was separated
  7. dry with materialdried over anhydrous sodium sulfate
  8. concentrationconcentrated
  9. customto give a residue
  10. customThe residue was purified by column chromatography (silica gel, petroleum ether/ethyl acetate=5:1)

출처 및 근거

ORD 기록
ord-06973f7ca4a84b699385c34c4f93b257
출처 데이터셋
uspto-grants-2016_08
특허 번호
US09422292B2

반응 노트

불러오는 중…