Tetrabutylammonium Fluoride → 2-[4-Hydroxy-2-(indol-2-ylthio)butyl]-4,4-dimethyl-2-oxazoline

1 ml of a 1M solution of tetra-n-butyl ammonium fluoride in tetrahydrofuran was added to a solution of 460 mg of 2-[4-tert-butyldiphenylsilyloxy-2-(indol-2-ylthio)butyl]-4,4-dimethyl-2-oxazoline [prepared as described in Example 78b)] in 20 ml of tetrahydrofuran, with stirring, at room temperature, and stirring was continued at this temperature for 30 minutes. After this time, the reaction mixture was diluted with water and then extracted with ethyl acetate. The ethyl acetate fraction was then washed with water and dried over anhydrous sodium sulfate. The solvent was then removed by evaporation under reduced pressure and the resulting residue was purified by silica gel column chromatography, using a mixture of 60% v/v ethyl acetate in hexane as the eluent, to afford 165 mg of the title compound as an oil.

1. customprepared
2. stirringstirring
3. extractionextracted with ethyl acetate
4. washThe ethyl acetate fraction was then washed with water
5. dry with materialdried over anhydrous sodium sulfate
6. customThe solvent was then removed by evaporation under reduced pressure
7. customthe resulting residue was purified by silica gel column chromatography
8. additiona mixture of 60% v/v ethyl acetate in hexane as the eluent

ORD record

ord-9f0f169c4ff2468abeea17578338d802

Source dataset

uspto-grants-1999_03

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05877199