Hydroxide → 4-oxo-3,4-dihydro-2H-1-benzopyran-2-carboxylic acid
Reaction equation
[O:1]=[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[O:5][CH:4]([C:12]([O:14]CC)=[O:13])[CH2:3]1.[OH-]>C(O)C>[O:1]=[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[O:5][CH:4]([C:12]([OH:14])=[O:13])[CH2:3]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The carboxylic acid group of the compound of Example 2 (ethyl 4-oxochromane-2-carboxylate) was treated with a metallic hydroxide base in ethanol, and then the aqueous layer was treated with an acid to form the free acid, which was washed with water and then dried to yield 3 g of 4-oxo-chromane-2-carboxylic acid.
Workup
- additionthe aqueous layer was treated with an acid
- customto form the free acid, which
- washwas washed with water
- customdried
Sources & evidence
- ORD record
- ord-5196757bd2644a829bbc28bfa7a7188e
- Source dataset
- uspto-grants-2004_06
- Patent number
- US06756403B2
Reaction notes
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