Hydrogen Peroxide → 1-methyl-1H-indol-6-ol

1-Methyl-1H-indol-6-yl-boronic acid (1.4 g, 8.0 mmol) was dissolved in ether (25 mL). Hydrogen peroxide (15%, 6 mL) was added over 5 minutes and the reaction mixture was stirred at room temperature for 1 h. The mixture was extracted with NaOH (1N, 2×50 mL) and the aqueous extracts were washed with ether (2×50 mL). The aqueous layers were cooled to 0° C. and acidified to pH 4.0 with 6 N HCl. The mixture was extracted with ether (3×100 mL) and the organic extracts were washed with water. The organic extracts were dried (MgSO4), filtered through a pad of silica gel and the pad was washed with ether (100 mL). After the filtrate was concentrated, the residue was chromatographed over silica gel with 10% to 20% ethyl acetate/hexanes to give 1-methyl-1H-indol-6-ol as a yellow solid (0.56 g, 47%).

1. extractionThe mixture was extracted with NaOH (1N, 2×50 mL)
2. washthe aqueous extracts were washed with ether (2×50 mL)
3. temperatureThe aqueous layers were cooled to 0° C.
4. extractionThe mixture was extracted with ether (3×100 mL)
5. washthe organic extracts were washed with water
6. dry with materialThe organic extracts were dried (MgSO4)
7. filtrationfiltered through a pad of silica gel
8. washthe pad was washed with ether (100 mL)
9. concentrationAfter the filtrate was concentrated
10. customthe residue was chromatographed over silica gel with 10% to 20% ethyl acetate/hexanes

ORDレコード

ord-8a2f46551c52460383671623af86216b

出典データセット

uspto-grants-2001_08

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US06281356B1