Basic information Safety Supplier Related

METHYL 3-AMINOPHENYLACETATE

Basic information Safety Supplier Related

METHYL 3-AMINOPHENYLACETATE Basic information

Product Name:
METHYL 3-AMINOPHENYLACETATE
Synonyms:
  • METHYL 3-AMINOPHENYLACETATE
  • 3-AMINOPHENYLACETIC ACID METHYL ESTER
  • methyl (3-aminophenyl)acetate(SALTDATA: FREE)
  • 3-Aminophenylacetic acid methyl ester, 3-(2-Methoxy-2-oxoethyl)aniline
  • Methyl 2-(3-aMinophenyl)acetate
  • 3-Aminophenylacetic acid methyl ester, 3-(2-Methoxy-2-oxoethyl)aniline, Methyl (3-aminophenyl)acetate
  • 3-aminoBenzeneacetic acid methyl ester
  • Benzeneacetic acid, 3-amino-, methyl ester
CAS:
52913-11-8
MF:
C9H11NO2
MW:
165.19
Mol File:
52913-11-8.mol
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METHYL 3-AMINOPHENYLACETATE Chemical Properties

Boiling point:
281.6±15.0 °C(Predicted)
Density 
1.143±0.06 g/cm3(Predicted)
storage temp. 
2-8°C(protect from light)
pka
4.17±0.10(Predicted)
form 
liquid
color 
Pale yellow
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Safety Information

Hazard Codes 
Xi
HS Code 
2916340000
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METHYL 3-AMINOPHENYLACETATE Usage And Synthesis

Synthesis

67-56-1

14338-36-4

52913-11-8

1. 3-Aminophenylacetic acid (15.5 g, 0.10 mol) was suspended in methanol (150 mL) and the mixture was cooled to 0°C. 2. Thionyl chloride (11.2 mL, 0.15 mol) was added slowly and dropwise with continuous stirring. 3. The reaction mixture gradually changed to a clarified orange solution with continued stirring for 4 hours. 4. Upon completion of the reaction, the solvent was removed by rotary evaporator. 5. The residual solid was dissolved in ethyl acetate (150 mL) and washed with saturated sodium bicarbonate solution (150 mL). 6. The organic phase is separated and washed sequentially with saturated sodium bicarbonate solution (100 mL) and brine, and finally dried over anhydrous sodium sulfate. 7. The desiccant was removed by filtration and the filtrate was concentrated under reduced pressure to give methyl 3-aminophenylacetate as a brown oil (14.1 g, 83% yield). 8. The product was analyzed by 1H NMR. 8. The product was characterized by 1H NMR (500 MHz, CDCl3): δ 7.12 (1H, dd), 6.7-6.6 (3H, m), 3.71 (3H, s), 3.55 (2H, s). 9. Follow-up step: conversion of methyl 3-aminophenylacetate to methyl (3-methylsulfonylamino-phenyl)-acetate.

References

[1] Patent: WO2009/53277, 2009, A1. Location in patent: Page/Page column 52
[2] Patent: WO2008/107365, 2008, A1. Location in patent: Page/Page column 83
[3] Patent: WO2005/19190, 2005, A2. Location in patent: Page/Page column 56
[4] Patent: WO2005/103050, 2005, A2. Location in patent: Page/Page column 171
[5] Patent: WO2004/41813, 2004, A1. Location in patent: Page 117

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