Ammonium Chloride → HCID 86730296, compound

HRID 1852450Notes

Reaction equation

HRID 1852450 reaction equation
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([C:8](=[O:12])[CH:9]([F:11])[F:10])=[N:6][CH:7]=1.[BH4-].[Na+].[NH4+].[Cl-]>CO>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([CH:8]([OH:12])[CH:9]([F:10])[F:11])=[N:6][CH:7]=1

Participants

5

Procedure

To a solution of 1-(5-bromopyridin-2-yl)-2,2-difluoroethanone (1.0 g, 4.2 mmol) in methanol (10 mL) was added NaBH4 (180 mg, 4.6 mmol) at 0° C. The resulting solution was stirred at ambient temperature for 2 hours before the addition of saturated aqueous NH4Cl (5 mL) at 0° C. Methanol was removed in vacuo, and the resulting aqueous solution was extracted with EtOAc (3×10 mL). The combined organic layers were washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo to afford the title compound as an off-white solid, which was used without further purification. 1H NMR (400 MHz, CDCl3) δ 8.70 (s, 1H), 7.91 (d, J=6.0 Hz, 1H), 7.52 (d, J=6.0 Hz, 1H), 5.89 (td, J=54.4, 3.9 Hz, 1H), 4.92-4.84 (m, 1H), 4.52 (br, 1H).

Workup

  1. customMethanol was removed in vacuo
  2. extractionthe resulting aqueous solution was extracted with EtOAc (3×10 mL)
  3. washThe combined organic layers were washed with brine
  4. dry with materialdried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-5be35269d01e49b3a404118ab942cd23
Source dataset
uspto-grants-2015_02
Patent number
US08962608B2

Reaction notes

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