Ethyl 5-hydroxyindole-2-carboxylate

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CAS:24985-85-1
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
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CAS:24985-85-1
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Products Intro: Product Name:Ethyl 5-hydroxyindole-2-carboxylate
CAS:24985-85-1

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Ethyl 5-hydroxyindole-2-carboxylate Basic information
Product Name:Ethyl 5-hydroxyindole-2-carboxylate
Synonyms:1H-Indole-2-carboxylic acid, 5-hydroxy-, ethyl ester;Ethyl 5-hydroxy-1H-indole-2-carboxylate;5-HYDROXYINDOLE-2-CARBOXYLIC ACID ETHYL ESTER;ETHYL 5-HYDROXYINDOLE-2-CARBOXYLATE;5-Hydroxy-2-indolecarboxylic acid ethyl ester;5-HYDOXYINDOLE-2-CARBOXYLIC ACID, ETHYL ESTER;2-CARBETHOXY-5-HYDROXYINDOLE;5-HO-ICA-OEt
CAS:24985-85-1
MF:C11H11NO3
MW:205.21
EINECS:246-554-9
Product Categories:Indoles and derivatives
Mol File:24985-85-1.mol
Ethyl 5-hydroxyindole-2-carboxylate Structure
Ethyl 5-hydroxyindole-2-carboxylate Chemical Properties
Melting point 150-151°C
Boiling point 410.4±25.0 °C(Predicted)
density 1.326±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Room Temperature
pka9.59±0.40(Predicted)
AppearanceOff-white to yellow Solid
Water Solubility Insoluble in water.
BRN 476925
CAS DataBase Reference24985-85-1(CAS DataBase Reference)
NIST Chemistry ReferenceEthyl 5-hydroxyindole-2-carboxylate(24985-85-1)
Safety Information
Safety Statements 22-24/25
MSDS Information
ProviderLanguage
ALFA English
Ethyl 5-hydroxyindole-2-carboxylate Usage And Synthesis
UsesEthyl 5-hydroxyindole-2-carboxylate is used as an important raw material and intermediate used in Organic Synthesis, Pharmaceuticals, Agrochemicals and Dyestuffs.
Synthesis
ETHYL 5-BENZYLOXYINDOLE-2-CARBOXYLATE

37033-95-7

Ethyl 5-hydroxyindole-2-carboxylate

24985-85-1

General procedure for the synthesis of ethyl 5-hydroxyindole-2-carboxylate from ethyl 5-benzyloxyindole-2-carboxylate: ethyl 5-benzyloxyindole-2-carboxylate (10 g, 34 mmol) was dissolved in ethanol (250 mL), 10% Pd/C catalyst was added, and the hydrogenation reaction was carried out for 20 h at atmospheric pressure (using a double-walled balloon). Upon completion of the reaction, the reaction mixture was diluted with ethyl acetate and filtered through diatomaceous earth to remove the catalyst. The filtrate was concentrated in vacuum to give ethyl 5-hydroxyindole-2-carboxylate (7 g, 99% yield) in brown solid form. The product was characterized by 1H NMR (400 MHz, CDCl3): δ 8.86 (broad peak, 1H), 7.29 (d, J = 8.80 Hz, 1H), 7.11 (s, 1H), 7.06 (s, 1H), 6.94 (d, J = 8.70 Hz, 1H), 4.83 (broad peak, 1H), 4.42 (q, J = 7.09 Hz, 2H ), 1.41 (t, J = 7.08Hz, 3H).

References[1] Journal of Medicinal Chemistry, 2003, vol. 46, # 1, p. 5 - 8
[2] Patent: US6670388, 2003, B1. Location in patent: Page column 6
[3] Patent: US6469046, 2002, B1
[4] Patent: US6608059, 2003, B1
[5] Journal of Medicinal Chemistry, 2014, vol. 57, # 24, p. 10455 - 10463
Tag:Ethyl 5-hydroxyindole-2-carboxylate(24985-85-1) Related Product Information
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