Sulfuric Acid → HCID 53401765, compound
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]=1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
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
- concentrationThe reaction mixture was concentrated
- washthe residue was washed with water
- dissolutionThe obtained white powder was dissolved in tetrahydrofuran (110 ml)
- addition1M diisobutylaluminum hydride/toluene solution (55 ml) was added dropwise at −78° C.
- stirringthe mixture was stirred at it
- customwas at −78° C. for 1 Saturated aqueous ammonium chloride solution
- additionwas added to the reaction mixture
- stirringthe mixture was stirred at room temperature
- filtrationAluminum salt was collected by filtration through celite
- extractionextracted with methylene chloride
- washwashed with saturated brine
- dry with materialdried over anhydrous sodium sulfate
- customThe solvent was evaporated under reduced pressure
- 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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