Ethyl 5-fluoropyridine-2-carboxylate → 5-Fluoropyridine-2-carboxaldehyde

HRID 1842552Notes

Reaction equation

HRID 1842552 reaction equation
[F:1][C:2]1[CH:3]=[CH:4][C:5]([C:8](OCC)=[O:9])=[N:6][CH:7]=1.[H-].C([Al+]CC(C)C)C(C)C>O1CCCC1>[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH:8]=[O:9])=[N:6][CH:7]=1

Participants

4

Procedure

To a solution of ethyl 5-fluoropyridine-2-carboxylate (25 g, 148 mmol) in tetrahydrofuran (250 mL) at −78° C. was added dropwise diisobutylaluminum hydride (1.0 M in hexanes; 296 mL, 296 mmol). After 1 h, the reaction was quenched with ethyl alcohol (10 mL). Saturated aqueous sodium potassium tartrate tetrahydrate (1.3 L) was added and the aqueous layer was extracted with ethyl acetate (2×). The combined organic extracts were washed with brine, dried over sodium sulfate, filtered. The solution mixture (1.4 L) was carried onto the next step without concentration. MS 125.9 (M+1).

Workup

  1. customthe reaction was quenched with ethyl alcohol (10 mL)
  2. additionSaturated aqueous sodium potassium tartrate tetrahydrate (1.3 L) was added
  3. extractionthe aqueous layer was extracted with ethyl acetate (2×)
  4. washThe combined organic extracts were washed with brine
  5. dry with materialdried over sodium sulfate
  6. filtrationfiltered
  7. concentrationThe solution mixture (1.4 L) was carried onto the next step without concentration

Sources & evidence

ORD record
ord-0782c9962f0f40fe82e755594cbf1cca
Source dataset
uspto-grants-2015_02
Patent number
US08946231B2

Reaction notes

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