ChemicalBook--->CAS DataBase List--->396091-50-2

396091-50-2

396091-50-2 Structure

396091-50-2 Structure
IdentificationBack Directory
[Name]

1H-Indole,5-(1-methylethoxy)-(9CI)
[CAS]

396091-50-2
[Synonyms]

396091-50-2
5-Isopropoxy-1H-indole
5-(Propan-2-yloxy)-1H-indole
1H-Indole, 5-(1-Methylethoxy)-
1H-Indole,5-(1-methylethoxy)-(9CI)
[Molecular Formula]

C11H13NO
[MDL Number]

MFCD13177542
[MOL File]

396091-50-2.mol
[Molecular Weight]

175.23
Chemical PropertiesBack Directory
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[Appearance]

Colorless to light yellow Liquid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2933998090
Spectrum DetailBack Directory
[Spectrum Detail]

1H-Indole,5-(1-methylethoxy)-(9CI)(396091-50-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-Iodopropane

75-30-9

5-Hydroxyindole

1953-54-4

1H-Indole,5-(1-methylethoxy)-(9CI)

396091-50-2

To a solution of 5-hydroxyindole (2.0 g, 0.015 mol) in acetonitrile (20 mL) was added anhydrous potassium carbonate (4 g, 0.028 mol) with vigorous stirring followed by 2-iodopropane (3 g, 0.018 mol). The reaction mixture was stirred at room temperature for 2 days, filtered and the solid was washed with acetonitrile. The filtrate was concentrated and purified by fast chromatography (80% hexane/20% ethyl acetate) to afford 5-isopropoxy-1H-indole (1.72 g, 83% yield) as a light yellow oil (M + 1 = 176.1).

[References]

[1] Patent: WO2005/9958, 2005, A1. Location in patent: Page 102
[2] Patent: US2005/288354, 2005, A1
[3] Journal of Medicinal Chemistry, 2007, vol. 50, # 12, p. 2865 - 2874
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