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Trimethylsilyldiazomethane → Methyl 2-Phenylisonicotinate

HRID 1171489
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1171489
[C:1]1([C:7]2[CH:8]=[C:9]([CH:13]=[CH:14][N:15]=2)[C:10]([OH:12])=[O:11])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH:16]1C=CC=CC=1.CO.C[Si](C=[N+]=[N-])(C)C>CCCCCC>[C:1]1([C:7]2[CH:8]=[C:9]([CH:13]=[CH:14][N:15]=2)[C:10]([O:12][CH3:16])=[O:11])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1
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Komponenten

5

Edukt 3

HCID 167693Trimethylsilyldiazomethane2×HCID 27628452-Phenylisonicotinic acidHCID 21927730Benzene methanol

Produkt 1

HCID 12183945Methyl 2-Phenylisonicotinate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8058HexaneLösungsmittel

Versuchsvorschrift

A solution of 2-phenylisonicotinic acid (459 mg, 2.30 mmol) in 9:1 benzene/methanol (20 mL) was cooled to 0° C., and treated with the dropwise addition of a 2.0 M hexane solution of (trimethylsilyl)diazomethane (1.15 mL, 2.30 mmol). The mixture was allowed to come to room temperature and stirred for 6 h. Analysis by TLC indicated incomplete reaction, so the mixture was treated with additional (trimethylsilyl)diazomethane solution (230 μL, 0.23 mmol), and the reaction was stirred for an additional 2 h. TLC of the mixture remained unchanged. The solvent was stripped, and the residue was partitioned between ethyl acetate and saturated sodium bicarbonate. The layers were separated, the organic phase was washed 2× with saturated sodium bicarbonate, the combined aqueous phases were extracted with ethyl acetate, and the combined organic phases were washed with brine, dried over sodium sulfate, and concentrated in vacuo. The residue was purified over silica gel, eluting with 20% ethyl acetate/heptane, to yield 372 mg of methyl 2-phenylisonicotinate as a colorless oil. 1H NMR (400 MHz, CDCl3) δ ppm 8.83 (d, J=5.27 Hz, 1H), 8.29 (s, 1H), 8.04 (d, J=7.03 Hz, 2H), 7.77 (d, J=3.52 Hz, 1H), 7.51-7.42 (m, 3H), 3.98 (s, 3H).

Aufarbeitung

  1. customto come to room temperature
  2. customreaction
  3. stirringthe reaction was stirred for an additional 2 h
  4. customthe residue was partitioned between ethyl acetate and saturated sodium bicarbonate
  5. customThe layers were separated
  6. washthe organic phase was washed 2× with saturated sodium bicarbonate
  7. extractionthe combined aqueous phases were extracted with ethyl acetate
  8. washthe combined organic phases were washed with brine
  9. dry with materialdried over sodium sulfate
  10. concentrationconcentrated in vacuo
  11. customThe residue was purified over silica gel
  12. washeluting with 20% ethyl acetate/heptane

Quellen und Nachweise

ORD-Eintrag
ord-fa4b79610ef343189093a43a0048f92a
Quelldatensatz
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07829571B2

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