Sulfuric Acid → HCID 67125523, compound
Reaction equation
[F:1][CH:2]([F:22])[O:3][C:4]1[C:9]2[O:10][C:11]3([O:17][C:8]=2[C:7]([C:18]([O:20]C)=[O:19])=[CH:6][CH:5]=1)[CH2:16][CH2:15][S:14][CH2:13][CH2:12]3.S(=O)(=O)(O)O>CO.C1COCC1.[OH-].[Li+]>[F:22][CH:2]([F:1])[O:3][C:4]1[C:9]2[O:10][C:11]3([O:17][C:8]=2[C:7]([C:18]([OH:20])=[O:19])=[CH:6][CH:5]=1)[CH2:16][CH2:15][S:14][CH2:13][CH2:12]3Participants
6
Reactant 2
Product 1
Reagents, catalysts & solvents 3
Procedure
Methyl 7-Difluoromethoxy-2′,3′,5′,6′-tetrahydro-spiro[1,3-benzodioxole-2,4′-(4H)-thiopyran]-4-carboxylate(437 mg) was dissolved in a mixture of Methanol(5 mL) and THF(5 mL) and 1M aqueous Lithium hydroxide(3.9 mL) was added. The ester was cleaved after 1 hour at 50° C. The solution was cooled to room temperature and acidified with 2N sulfuric acid (1.95 mL) and the product was extracted into EtOAc. 7-Difluoromethoxy-2′,3′,5′,6′-tetrahydro-spiro[1,3-benzodioxole-2,4′-(4H)-thiopyran]-4-carboxylic acid was obtained after removal of solvents under reduced pressure.
Workup
- additionwas added
- extractionthe product was extracted into EtOAc
Sources & evidence
- ORD record
- ord-81c8bd930d794650b7473a6b81ef6294
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08980905B2
Reaction notes
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