Sulfuric Acid → HCID 524516, compound

HRID 713997Notes

Reaction equation

HRID 713997 reaction equation
[CH3:1][N:2]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3]1.OS(O)(=O)=O.[H][H]>C(O)C.O=[Pt]=O>[CH3:1][N:2]1[CH:10]2[CH:5]([CH2:6][CH2:7][CH2:8][CH2:9]2)[CH2:4][CH2:3]1

Participants

6

Conditions

Temperature
100 °C

Procedure

To a solution of 100 g of 1-methylindole in absolute ethanol in a 600 mL autoclave, 5 g of PtO2 and 10 mL of H2SO4 were added. The mixture was sealed and pressurized with hydrogen to 1500 psig. The reaction mixture was heated at 100° C. overnight while stirring at about 400 rpm. The reaction mixture was pressurized again to 1500 psig and heated at 100° C. for several more hours. The reaction mixture was cooled and filtered to remove the catalyst. The filtrate was concentrated on a rotary evaporator to remove ethanol. The residue was neutralized with sodium hydroxide solution and left to stir at room temperature for about 30 minutes. The solution was transferred to a reparatory funnel and extracted with diethyl ether. The ether layer was dried over anhydrous MgSO4, filtered and concentrated at reduced pressure on a rotary evaporator to give 93.0 g of the product, 1-methyl-octahydroindole, as a yellow oil. The product was confirmed by NMR.

Workup

  1. customThe mixture was sealed
  2. temperatureheated at 100° C. for several more hours
  3. temperatureThe reaction mixture was cooled
  4. filtrationfiltered
  5. customto remove the catalyst
  6. concentrationThe filtrate was concentrated on a rotary evaporator
  7. customto remove ethanol
  8. waitleft
  9. stirringto stir at room temperature for about 30 minutes
  10. customThe solution was transferred to a reparatory funnel
  11. extractionextracted with diethyl ether
  12. dry with materialThe ether layer was dried over anhydrous MgSO4
  13. filtrationfiltered
  14. concentrationconcentrated at reduced pressure on a rotary evaporator

Sources & evidence

ORD record
ord-babd31a93161425a8b6eb35716be2004
Source dataset
uspto-grants-2015_11
Patent number
US09187334B2

Reaction notes

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