Potassium Carbonate → Ammonium Hydroxide

HRID 564486Notes

Reaction equation

HRID 564486 reaction equation
Cl.Br[C:3]1[CH:4]=[C:5]([CH2:10][NH2:11])[CH:6]=[CH:7][C:8]=1[F:9].[OH:12][CH2:13][C:14]1[CH:15]=[C:16](B(O)O)[CH:17]=[CH:18][CH:19]=1.C(=O)([O-])[O-].[K+].[K+]>O1CCOCC1.O.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[NH4+:11].[OH-:12].[NH2:11][CH2:10][C:5]1[CH:6]=[CH:7][C:8]([F:9])=[C:3]([C:18]2[CH:17]=[CH:16][CH:15]=[C:14]([CH2:13][OH:12])[CH:19]=2)[CH:4]=1

Participants

8

Procedure

[(3-Bromo-4-fluorophenyl)methyl]amine hydrochloride (0.795 g, 3.29 mmol), [3-(hydroxymethyl)phenyl]boronic acid (0.5 g, 3.29 mmol), potassium carbonate (2.275 g, 16.5 mmol), and tetrakis(triphenylphosphine)palladium(0) (0.114 g, 0.1 mmol) were combined in dioxane (10 mL) and water (3 mL). The mixture was microwaved at 150° C. for 30 min. The solvents were concentrated and the residue taken up in EtOAc and H2O. The aqueous phase was extracted 2× with EtOAc. The combined organic phases were dried over anhydrous Na2SO4, filtered and concentrated. The residue was purified by CombiFlash on a silica gel column eluted with 0-100% CH2Cl2/CH2Cl2: 20% MeOH: 1% NH4OH to afford the title compound as viscous oil. LC-MS m/z 231.8 (M+H)+, 1.03 min (ret time).

Workup

  1. customThe mixture was microwaved at 150° C. for 30 min
  2. concentrationThe solvents were concentrated
  3. extractionThe aqueous phase was extracted 2× with EtOAc
  4. dry with materialThe combined organic phases were dried over anhydrous Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe residue was purified by CombiFlash on a silica gel column
  8. washeluted with 0-100% CH2Cl2/CH2Cl2

Sources & evidence

ORD record
ord-add08b7f91cf41c79c4d6e76bef879dd
Source dataset
uspto-grants-2011_11
Patent number
US08067408B2

Reaction notes

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