反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
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
后处理
- 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))