Sulfuric Acid → HCID 53401765, compound

HRID 1093487Notes

Reaction equation

HRID 1093487 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]=[CH:9][C:10](O)=[O:11])=[CH:4][CH:3]=1.S(=O)(=O)(O)O>CO>[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH:8]=[CH:9][CH2:10][OH:11])=[CH:6][CH:7]=1

Participants

4

Conditions

Temperature
100 °C

Procedure

3-(4-Fluorophenyl)acrylic acid (5.0 g) was dissolved in methanol (30 ml), concentrated sulfuric acid (0.5 ml) was added, and the mixture was stirred at 100° C. for 3.5 hr. The reaction mixture was concentrated, and the residue was washed with water. The obtained white powder was dissolved in tetrahydrofuran (110 ml), 1M diisobutylaluminum hydride/toluene solution (55 ml) was added dropwise at −78° C., and the mixture was stirred at it was at −78° C. for 1 Saturated aqueous ammonium chloride solution was added to the reaction mixture, and the mixture was stirred at room temperature. Aluminum salt was collected by filtration through celite, extracted with methylene chloride, washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was washed with water and hexane to give the object product (3.82 g) as a white powder.

Workup

  1. concentrationThe reaction mixture was concentrated
  2. washthe residue was washed with water
  3. dissolutionThe obtained white powder was dissolved in tetrahydrofuran (110 ml)
  4. addition1M diisobutylaluminum hydride/toluene solution (55 ml) was added dropwise at −78° C.
  5. stirringthe mixture was stirred at it
  6. customwas at −78° C. for 1 Saturated aqueous ammonium chloride solution
  7. additionwas added to the reaction mixture
  8. stirringthe mixture was stirred at room temperature
  9. filtrationAluminum salt was collected by filtration through celite
  10. extractionextracted with methylene chloride
  11. washwashed with saturated brine
  12. dry with materialdried over anhydrous sodium sulfate
  13. customThe solvent was evaporated under reduced pressure
  14. washThe residue was washed with water and hexane

Sources & evidence

ORD record
ord-3dc546db5ba8439da89b3018e6606e4b
Source dataset
uspto-grants-2012_03
Patent number
US08129361B2

Reaction notes

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