Methanol → (5-(Trifluoromethyl)pyridin-2-yl)methanol

HRID 1750530Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1750530
I[C:2]1[CH:7]=[CH:6][C:5]([C:8]([F:11])([F:10])[F:9])=[CH:4][N:3]=1.[Li]CCCC.CCCCCC.[BH4-].[Na+].[Cl-].[NH4+].[CH3:27][OH:28]>C1(C)C=CC=CC=1.CN(C=O)C>[F:9][C:8]([F:11])([F:10])[C:5]1[CH:6]=[CH:7][C:2]([CH2:27][OH:28])=[N:3][CH:4]=1

Komponenten

9

Reaktionsbedingungen

Temperatur
-78 °C

Versuchsvorschrift

To the solution of 2-iodo-5-(trifluoromethyl)pyridine (CAS number 100366-75-4; 10 g, 69.4 mmol) in toluene (250 ml) at −78° C. was added n-BuLi in hexane (2.5 M, 15.0 mL, 37.5 mmol). The reaction was stirred at −78° C. for 15 minutes. To this was then added drop wise DMF (3.5 ml) and then stirred at −78° C. for 1 hour. Sodium borohydride (2.74 g, 72.0 mmol) and methanol (50 ml) were added and the resulting reaction mixture was stirred for 30 minutes and then allowed to warm to room temperature. The reaction was cooled to −10° C. and to this was then added a saturated solution of ammonium chloride. The organics were extracted with ethyl acetate (2×200 ml) and the combined organics were washed with brine, dried over sodium sulfate and concentrated in vacuo to afford the title compound which was used without further purification.

Aufarbeitung

  1. stirringstirred at −78° C. for 1 hour
  2. customthe resulting reaction mixture
  3. stirringwas stirred for 30 minutes
  4. temperatureto warm to room temperature
  5. temperatureThe reaction was cooled to −10° C.
  6. extractionThe organics were extracted with ethyl acetate (2×200 ml)
  7. washthe combined organics were washed with brine
  8. dry with materialdried over sodium sulfate
  9. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-8996f018033549598783e35e5a0c1197
Quelldatensatz
uspto-grants-2015_10
Patentnummer
US09156829B2

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