Basic information Safety Supplier Related

methyl 3-amino-5-chlorobenzoate

Basic information Safety Supplier Related

methyl 3-amino-5-chlorobenzoate Basic information

Product Name:
methyl 3-amino-5-chlorobenzoate
Synonyms:
  • methyl 3-amino-5-chlorobenzoate
  • Benzoic acid, 3-aMino-5-chloro-, Methyl ester
  • Methyl3-amino-5-chlorobenzoate98%
  • 3-AMINO-5-CHLORO-BENZOIC ACID METHYL ESTER
  • Methyl 3-amino-5-chlorobenzoate 98%
CAS:
21961-31-9
MF:
C8H8ClNO2
MW:
185.61
Mol File:
21961-31-9.mol
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methyl 3-amino-5-chlorobenzoate Chemical Properties

Boiling point:
329.4±22.0 °C(Predicted)
Density 
1.311±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
2.39±0.10(Predicted)
Appearance
White to yellow Solid
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Safety Information

HS Code 
2916399090
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methyl 3-amino-5-chlorobenzoate Usage And Synthesis

Synthesis

36138-28-0

21961-31-9

Step 2: Synthesis of methyl 3-amino-5-chlorobenzoate A dioxane solution (0.13 M) of methyl 3-chloro-5-nitrobenzoate (from Step 1) was placed in a reaction flask and SnCl2 (3.9 equiv) was added. The reaction mixture was stirred at 70 °C for 2 hours. After completion of the reaction, it was cooled to room temperature and EtOAc and saturated aqueous NaHCO3 solution was added. The reaction mixture was filtered to remove the precipitate formed. The aqueous phase was separated and extracted with EtOAc. All organic layers were combined and dried with anhydrous Na2SO4. Evaporation of the solvent under reduced pressure afforded the title compound methyl 3-amino-5-chlorobenzoate in 88% yield as a yellow solid. Mass spectrum (ES+) m/z 186,188 (M+H)+.

References

[1] Patent: WO2007/28789, 2007, A1. Location in patent: Page/Page column 35
[2] Patent: US2010/261687, 2010, A1. Location in patent: Page/Page column 60

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