반응 #474433

반응 방정식

NaOH

1-(1,1-dimethylethyl) 7-methyl 5-bromo-3-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)-1H-indole-1,7-dicarboxylate

1-(1,1-dimethylethyl) 7-ethyl 5-bromo-3-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)-1H-indole-1,7-dicarboxylate

→

5-Bromo-3-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)-1H-indole-7-carboxylic acid

용매

MeOH

water

반응 조건

후처리

1. 1
   기타fitted with a reflux condenser
2. 2
   기타The MeOH was removed by rotovap
3. 3
   workup.ADDITIONa solution of 6 M HCl was added until the mixture
4. 4
   여과The yellow solid was filtered off
5. 5
   추출the filtrate was extracted with EtOAc (3×10 mL)
6. 6
   건조The combined organic layers were dried (Na2SO4)
7. 7
   농축concentrated under reduced pressure
8. 8
   여과the residue was combined with the precipitate from the filtration
9. 9
   기타dried under house vacuum at 45° C. overnight
10. 10
    기타Recovered 2.98 g (86%) of the title compound

실험 절차

A solution of 6 M NaOH (12 mL, 72.0 mmol) was added to a suspension of 1-(1,1-dimethylethyl) 7-methyl 5-bromo-3-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)-1H-indole-1,7-dicarboxylate (0.93 g, 1.912 mmol) and 1-(1,1-dimethylethyl) 7-ethyl 5-bromo-3-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)-1H-indole-1,7-dicarboxylate (3.08 g, 6.16 mmol) in MeOH (50 mL) and water (25 mL) in a 250 mL round bottomed flask fitted with a reflux condenser. The reaction was heated at 85° C. (bath temp) for 1.5 h. The MeOH was removed by rotovap, and a solution of 6 M HCl was added until the mixture had attained a pH of ˜1 by pH paper. The yellow solid was filtered off, and the filtrate was extracted with EtOAc (3×10 mL). The combined organic layers were dried (Na2SO4) and concentrated under reduced pressure, and the residue was combined with the precipitate from the filtration and dried under house vacuum at 45° C. overnight. Recovered 2.98 g (86%) of the title compound.

출처