Reaction equation
[OH:1][C:2]1([C:18]([O:20]C)=[O:19])[C:11]2[C:6](=[C:7]([O:13][C:14]([F:17])([F:16])[F:15])[CH:8]=[C:9]([Cl:12])[CH:10]=2)[O:5][CH2:4][CH2:3]1.[OH-].[K+].O>C(O)(C)C>[OH:1][C:2]1([C:18]([OH:20])=[O:19])[C:11]2[C:6](=[C:7]([O:13][C:14]([F:17])([F:15])[F:16])[CH:8]=[C:9]([Cl:12])[CH:10]=2)[O:5][CH2:4][CH2:3]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 4-hydroxy-6-chloro-8-trifluoromethoxychroman-4-yl carboxylic acid, methyl ester in iso-propanol (50 mL) was added to KOH/H2O (20%, 60 mL) and the mixture was refluxed overnight. The resultant solution was partially concentrated, and the remainder was acidified with H2SO4 (10%). The very turbid mixture was extracted with ether (3×), and the combined organic phase was dried (Na2SO4) and concentrated. The crude product was purified via prep-HPLC (CH3CN:0.1M ammonium acetate (30:60)). The fractions of interest were partly concentrated and extracted with ether. The combined organic layers were washed with water, dried (Na2SO4), and concentrated, yielding 0.24 g (10% over steps (vi)-(ix)).
Workup
- temperaturethe mixture was refluxed overnight
- concentrationThe resultant solution was partially concentrated
- extractionThe very turbid mixture was extracted with ether (3×)
- dry with materialthe combined organic phase was dried (Na2SO4)
- concentrationconcentrated
- customThe crude product was purified via prep-HPLC (CH3CN:0.1M ammonium acetate (30:60))
- concentrationThe fractions of interest were partly concentrated
- extractionextracted with ether
- washThe combined organic layers were washed with water
- dry with materialdried (Na2SO4)
- concentrationconcentrated
- customyielding 0.24 g (10% over steps (vi)-(ix))
Sources & evidence
- ORD record
- ord-c0de8a02ad934412b2796506b0bef1b1
- Source dataset
- uspto-grants-2004_06
- Patent number
- US06750243B1
Linked notes
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