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Trimethylsilyldiazomethane → Methyl 2-Phenylisonicotinate

HRID 1374258
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1374258
[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

Preparation H1, Step 2: 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. customPreparation H1, Step 2
  2. customto come to room temperature
  3. customreaction
  4. stirringthe reaction was stirred for an additional 2 h
  5. customthe residue was partitioned between ethyl acetate and saturated sodium bicarbonate
  6. customThe layers were separated
  7. washthe organic phase was washed 2× with saturated sodium bicarbonate
  8. extractionthe combined aqueous phases were extracted with ethyl acetate
  9. washthe combined organic phases were washed with brine
  10. dry with materialdried over sodium sulfate
  11. concentrationconcentrated in vacuo
  12. customThe residue was purified over silica gel
  13. washeluting with 20% ethyl acetate/heptane

Quellen und Nachweise

ORD-Eintrag
ord-6ef711e8dd37421a9ddfde4b2321820e
Quelldatensatz
uspto-grants-2007_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07163937B2

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