Sulfuric Acid → HCID 361174, compound

HRID 1093486Notes

Reaction equation

HRID 1093486 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10](O)=[O:11])[CH:5]=[CH:6][CH:7]=1.S(=O)(=O)(O)O>CO>[Cl:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][CH2:10][OH:11])[CH:5]=[CH:6][CH:7]=1

Participants

4

Conditions

Temperature
100 °C

Procedure

3-(3-Chlorophenyl)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 1.5 hr. The reaction mixture was concentrated, and the residue was washed with water. The obtained pale-yellow powder was dissolved in methylene chloride (130 ml), 1M diisobutylaluminum hydride/toluene solution (52 ml) was added dropwise at −78° C., and the mixture was stirred as it was at −78° C. for 2 hr. 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 purified by silica gel column chromatography (hexane:ethyl acetate) to give the object product (3.29 g) as a yellow oil.

Workup

  1. concentrationThe reaction mixture was concentrated
  2. washthe residue was washed with water
  3. dissolutionThe obtained pale-yellow powder was dissolved in methylene chloride (130 ml)
  4. addition1M diisobutylaluminum hydride/toluene solution (52 ml) was added dropwise at −78° C.
  5. stirringthe mixture was stirred as it
  6. waitwas at −78° C. for 2 hr
  7. additionSaturated aqueous ammonium chloride solution was 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. customThe residue was purified by silica gel column chromatography (hexane:ethyl acetate)

Sources & evidence

ORD record
ord-cf773ccac9ac45cc989f6d1b49593271
Source dataset
uspto-grants-2012_03
Patent number
US08129361B2

Reaction notes

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