Cesium fluoride → 7-Fluoro-2,3-dihydrobenzofuran-3-ol

HRID 1025488Notes

Reaction equation

HRID 1025488 reaction equation
[F:1][C:2]1[C:3]([O:10][CH2:11][Si](C)(C)C)=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH:5]=[O:6].[F-].[Cs+]>CN(C=O)C.C([O-])(O)=O.[Na+]>[F:1][C:2]1[C:3]2[O:10][CH2:11][CH:5]([OH:6])[C:4]=2[CH:7]=[CH:8][CH:9]=1

Participants

5

Conditions

Temperature
95 °C

Procedure

A mixture of 3-fluoro-2-((trimethylsilyl)methoxy)benzaldehyde (6.75 g, 29.8 mmol) and CsF (13.73 g, 90 mmol) in DMF (88 mL) were heated in 95° C. oil bath for 3 days. At the conclusion of this period, the reaction was analyzed by HPLC, which showed the starting material had disappeared. The reaction mixture was cooled to rt, diluted with aqueous NaHCO3 and extracted with Et2O (3×15 mL), followed by EtOAc (3×15 mL). The combined organic layers were washed with water (25 mL), brine (25 mL), dried (MgSO4), and concentrated to afford Compound 1B as a brown oil (4.6 g). The crude product was used in next step without further purification.

Workup

  1. temperatureThe reaction mixture was cooled to rt
  2. extractionextracted with Et2O (3×15 mL)
  3. washThe combined organic layers were washed with water (25 mL), brine (25 mL)
  4. dry with materialdried (MgSO4)
  5. concentrationconcentrated

Sources & evidence

ORD record
ord-9c88fe72201e49e7aa61a1a28abd5fe8
Source dataset
uspto-grants-2014_05
Patent number
US08729084B2

Reaction notes

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