Hydrochloric Acid → HCID 57584092, compound
Reaction equation
Cl.[O:2]=[C:3]1[C:8]([C:9]2[CH:18]=[CH:17][C:12]([C:13]([O:15]C)=[O:14])=[CH:11][CH:10]=2)=[CH:7][CH:6]=[CH:5][O:4]1>O>[O:2]=[C:3]1[C:8]([C:9]2[CH:18]=[CH:17][C:12]([C:13]([OH:15])=[O:14])=[CH:11][CH:10]=2)=[CH:7][CH:6]=[CH:5][O:4]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 90 °C
Procedure
An aqueous 6 N hydrochloric acid solution (5 mL) was added to methyl 4-(2-oxo-2H-pyran-3-yl)benzoate (72 mg), followed by stirring at 90° C. for 15 hours. The reaction mixture was cooled to room temperature, water was added, and the solid was collected by filtration. After washing with water, this solid was dried under reduced pressure to obtain 4-(2-oxo-2H-pyran-3-yl)benzoic acid (65 mg) as a pale brown solid.
Workup
- temperatureThe reaction mixture was cooled to room temperature
- filtrationthe solid was collected by filtration
- washAfter washing with water
- customthis solid was dried under reduced pressure
Sources & evidence
- ORD record
- ord-3c993bb5180242b2ad2a5a947b7a5624
- Source dataset
- uspto-grants-2011_09
- Patent number
- US08022208B2
Reaction notes
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