Sodium Iodide → 5-Ethyl-2-pyridinol

HRID 859732Notes

Reaction equation

HRID 859732 reaction equation
C[O:2][C:3]1[CH:8]=[CH:7][C:6]([CH:9]=[CH2:10])=[CH:5][N:4]=1.[Na+].[I-]>CO.[Pd]>[CH2:9]([C:6]1[CH:7]=[CH:8][C:3](=[O:2])[NH:4][CH:5]=1)[CH3:10]

Participants

5

Conditions

Temperature
65 °C

Procedure

To a solution of 2-methoxy-5-vinyl-pyridine (2 g) in anhydrous MeOH was added Pd/C (10 wt %, 100 mg). The mixture was stirred under H2 atmosphere for 5 hours before it was filtered through a pad of celite. The solvent was removed in vacuo and the residue was taken directly into next step without further purification. The crude product from previous step was dissolved in anhydrous MeCN. To this solution was added NaI (3.3 g, 21.9 mmol) and TMSCI (2.8 mL, 21.9 mmol). The resulting mixture was heated to 65° C. for 5 hours before it was filtered through a pad of celite. The filtrate was concentrated in vacuo and the residue was purified by flash column chromatography to afford the desired product (1.5 g, 83% yield). 1H NMR (300 MHz, CDCl3): δ 1.17 (t, J=7.5 Hz, 3 H), 2.39–2.49 (m, 2 H), 6.50–6.58 (m, 1 H), 7.15 (s, 1 H), 7.35–7.45 (m, 1 H).

Workup

  1. filtrationwas filtered through a pad of celite
  2. customThe solvent was removed in vacuo
  3. customthe residue was taken directly into next step without further purification
  4. dissolutionThe crude product from previous step was dissolved in anhydrous MeCN
  5. filtrationwas filtered through a pad of celite
  6. concentrationThe filtrate was concentrated in vacuo
  7. customthe residue was purified by flash column chromatography

Sources & evidence

ORD record
ord-9923e0ec42be470ea936ae5003bc2c83
Source dataset
uspto-grants-2006_12
Patent number
US07151105B2

Reaction notes

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