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Acetic acid 1H-indol-4-yl ester

4-indolyl acetate

CAS: 5585-96-6

Molecular Formula: C10H9NO2

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Acetic acid 1H-indol-4-yl ester - Names and Identifiers

Name 4-indolyl acetate
Synonyms ACETOXYINDOLE
4-ACETOXYINDOLE
4-Acetoxyindole
4-indolyl acetate
4-INDOLYL ACETATE
4-INDOXYL ACETATE
4-Indoxyl acetate
4-Acetoxy-1H-indole
1H-indol-4-yl acetate
1H-Indol-4-ol,4-acetate
Acetic acid 1H-indol-4-yl ester
CAS 5585-96-6
EINECS 1312995-182-4
InChI InChI=1/C10H9NO2/c1-7(12)13-10-4-2-3-9-8(10)5-6-11-9/h2-6,11H,1H3
InChIKey ZXDMUHFTJWEDEF-UHFFFAOYSA-N

Acetic acid 1H-indol-4-yl ester - Physico-chemical Properties

Molecular FormulaC10H9NO2
Molar Mass175.18
Density1?+-.0.06 g/cm3(Predicted)
Melting Point100-102°C
Boling Point339.1±15.0 °C(Predicted)
Flash Point158.9°C
Solubility Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
Vapor Presure9.41E-05mmHg at 25°C
AppearanceSolid
ColorOff-White to Beige
pKa16.38±0.30(Predicted)
Storage Condition2-8°C
Refractive Index1.633
MDLMFCD00010678

Acetic acid 1H-indol-4-yl ester - Risk and Safety

Hazard SymbolsXi - Irritant
Irritant
WGK Germany3
Hazard NoteIrritant

Acetic acid 1H-indol-4-yl ester - Reference Information

Use 4-acetoxyindole is an organic intermediate, it can be obtained by acylation of 4-hydroxyindole with acetic anhydride.
preparation 4-hydroxyindole (1 equivalent of the limiting reagent) was loaded into a vessel under N2, DCM (dichloromethane; 6 volumes based on 4-hydroxyindole loading) was then loaded. The reaction was cooled to 0-5 °c and pyridine (1.2 eq.) was added dropwise at 0-5 °c. Acetic anhydride (1.1 equiv.) was added dropwise at 0-5 °c and the reaction was warmed to 20-25 °c for 1-1.5 hours and stirred at 20-25 °c for an additional 3 hours. The reaction was sampled and analyzed for completion. The reaction was then washed three times with a 20% aqueous citric acid solution (based on 4-hydroxyindole loading, 3x 3 volumes) and with saturated NaHCO3 (based on 4-hydroxyindole loading, 3 volumes) wash once. The DCM solution was dried over MgSO4 and filtered, and the DCM layer was concentrated to half volume by distillation. Heptane (6 vol based on 4-hydroxyindole loading) was added and additional DCM was removed by distillation until complete precipitation of stage 1 occurred. The reaction was cooled to 15-25 °c and the solid was collected by filtration, washed with heptane (1 Vol based on 4-hydroxyindole loading), drying at 60 °c under vacuum overnight gave 4-acetoxyindole.
Last Update:2024-04-09 02:00:09
Acetic acid 1H-indol-4-yl ester
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View History
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