4-FLUORO-7-INDOLE CARBOXYLIC ACID METHYL ESTER

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4-FLUORO-7-INDOLE CARBOXYLIC ACID METHYL ESTER Basic information
Product Name:4-FLUORO-7-INDOLE CARBOXYLIC ACID METHYL ESTER
Synonyms:1H-Indole-7-carboxylic acid, 4-fluoro-, Methyl ester;4-FLUORO-7-INDOLE CARBOXYLIC ACID METHYL ESTER;Methyl 4-Fluoroindole-7-carboxylate;Methyl 4-fluoro-1H-indole-7-carboxylate
CAS:313337-35-8
MF:C10H8FNO2
MW:193.17
EINECS:
Product Categories:
Mol File:313337-35-8.mol
4-FLUORO-7-INDOLE CARBOXYLIC ACID METHYL ESTER Structure
4-FLUORO-7-INDOLE CARBOXYLIC ACID METHYL ESTER Chemical Properties
Boiling point 335.6±22.0 °C(Predicted)
density 1.341±0.06 g/cm3(Predicted)
storage temp. 2-8°C
pka14.82±0.30(Predicted)
AppearanceWhite to off-white Solid
Safety Information
MSDS Information
4-FLUORO-7-INDOLE CARBOXYLIC ACID METHYL ESTER Usage And Synthesis
Synthesis
4-fluoro-1H-indole-7-carboxylic acid

313337-34-7

(TRIMETHYLSILYL)DIAZOMETHANE

18107-18-1

4-FLUORO-7-INDOLE CARBOXYLIC ACID METHYL ESTER

313337-35-8

To a suspension of 4-fluoro-7-carboxyindole in a solvent mixture of methanol (18 mL) and benzene (62 mL), (trimethylmethylsilyl) diazomethane (8.8 mL, 17.6 mmol, 2 M hexane solution) was slowly added. The reaction mixture was stirred at room temperature for 30 min, followed by quenching the reaction with excess acetic acid. The reaction solution was concentrated in vacuum and the resulting crude product was purified by fast column chromatography using gradient elution (hexane to 10% ethyl acetate/hexane) as eluent to give the final methyl 4-fluoro-1H-indole-7-carboxylate as a white solid (1.04 g, 83% yield in two steps).

References[1] Patent: US2004/6090, 2004, A1. Location in patent: Page/Page column 33
[2] Patent: WO2004/11425, 2004, A2. Location in patent: Page 73
4-FLUORO-7-INDOLE CARBOXYLIC ACID METHYL ESTER Preparation Products And Raw materials
Raw materials4-fluoro-1H-indole-7-carboxylic acid-->(TRIMETHYLSILYL)DIAZOMETHANE
Tag:4-FLUORO-7-INDOLE CARBOXYLIC ACID METHYL ESTER(313337-35-8) Related Product Information
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