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Potassium Fluoride → 2-Amino-3-nitro-5-propenyl-benzoic acid methyl ester

HRID 1845044
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HRID 1845044 반응식
[CH3:1][O:2][C:3](=[O:15])[C:4]1[CH:9]=[C:8](Br)[CH:7]=[C:6]([N+:11]([O-:13])=[O:12])[C:5]=1[NH2:14].[CH2:16]([Sn](CCCC)(CCCC)C=CC)[CH2:17][CH2:18]C.[F-].[K+]>O1CCOCC1>[CH3:1][O:2][C:3](=[O:15])[C:4]1[CH:9]=[C:8]([CH:16]=[CH:17][CH3:18])[CH:7]=[C:6]([N+:11]([O-:13])=[O:12])[C:5]=1[NH2:14]
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참가 물질

5

반응물 3

HCID 522689Potassium FluorideHCID 17984898Methyl 2-amino-5-bromo-3-nitrobenzoateHCID 57369809Stannane, tributyl-1-propenyl-

생성물 1

HCID 669404292-Amino-3-nitro-5-propenyl-benzoic acid methyl ester수율 77%

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

A solution of 0.5 g (1.8 mmol) of the above ester 0.9 g (2.7 mmol) of tributyl-propenyl-stannane, 0.18 g (0.18 mmol mmol) of (tetrakistriphenyl phosphine) palladium (0) in 25 mL of dioxane was degassed with nitrogen for 20 min then refluxed under nitrogen for 12 h. The reaction mixture was cooled, 20 mL of 2 M KF solution was added. The mixture was stirred for 20 min, extracted with ethyl acetate washed with water and brine. The residue was purified by column chromatography using 8:2 hexane and ethyl acetate to afford 0.35 g (77%) of the 2-amino-3-nitro-5-propenyl-benzoic acid methyl ester as a solid LCMS: 239 (M+1)+.

후처리

  1. temperaturethen refluxed under nitrogen for 12 h
  2. temperatureThe reaction mixture was cooled
  3. extractionextracted with ethyl acetate
  4. washwashed with water and brine
  5. customThe residue was purified by column chromatography

출처 및 근거

ORD 기록
ord-6bdfe0f4dab243589d51e38ebbb67b16
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08946259B2

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