Hydrochloric Acid → HCID 57655997, compound

HRID 2041152Notes

Reaction equation

HRID 2041152 reaction equation
[F:1][C:2]([F:15])([F:14])[C:3]([NH:5][CH2:6][C:7]1[CH:12]=[CH:11][C:10]([OH:13])=[CH:9][CH:8]=1)=[O:4].Br[CH2:17][C:18](=[O:23])[C:19]([CH3:22])([CH3:21])[CH3:20].C(=O)([O-])[O-].[K+].[K+].[I-].[K+].Cl>CC(C)=O>[CH3:20][C:19]([CH3:22])([CH3:21])[C:18](=[O:23])[CH2:17][O:13][C:10]1[CH:11]=[CH:12][C:7]([CH2:6][NH:5][C:3](=[O:4])[C:2]([F:14])([F:15])[F:1])=[CH:8][CH:9]=1

Participants

7

Procedure

Mix 2,2,2-trifluoro-N-(4-hydroxy-benzyl)-acetamide (438 mg, 2.0 mmol), 1-bromopinacolone (430 mg, 2.4 mmol), anhydrous potassium carbonate (829 mg, 6.0 mmol) and potassium iodide (33 mg, 0.1 mmol) with acetone. Heat under reflux for 12 h. Acidify with 1N aqueous HCl and extract with EtOAc three times. Combine the organic extracts, wash with brine, dry over Na2SO4, filter and concentrate. Purify by chromatography on silica gel eluting with EtOAc/hexane (1:3) to give the desired intermediate as a colorless oil. MS (ES+) m/z: 335 (M+NH4)+. MS (ES−) m/z: 316 (M−H)−.

Workup

  1. temperatureHeat
  2. temperatureunder reflux for 12 h
  3. extractionextract with EtOAc three times
  4. washCombine the organic extracts, wash with brine
  5. dry with materialdry over Na2SO4
  6. filtrationfilter
  7. concentrationconcentrate
  8. customPurify by chromatography on silica gel eluting with EtOAc/hexane (1:3)

Sources & evidence

ORD record
ord-19df08e81ab44db88f32b7e52dbb931d
Source dataset
uspto-grants-2013_11
Patent number
US08580780B2

Reaction notes

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