Basic information Safety Supplier Related

2-NITRO-3-AMINO-4-METHYLBENZOIC ACID

Basic information Safety Supplier Related

2-NITRO-3-AMINO-4-METHYLBENZOIC ACID Basic information

Product Name:
2-NITRO-3-AMINO-4-METHYLBENZOIC ACID
Synonyms:
  • 3-AMINO-4-METHYL-2-NITROBENZOIC ACID
  • 2-NITRO-3-AMINO-4-METHYLBENZOIC ACID
  • Benzoic acid, 3-amino-4-methyl-2-nitro-
CAS:
37901-90-9
MF:
C8H8N2O4
MW:
196.16
Product Categories:
  • API intermediates
Mol File:
37901-90-9.mol
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2-NITRO-3-AMINO-4-METHYLBENZOIC ACID Chemical Properties

Boiling point:
444.8±45.0 °C(Predicted)
Density 
1.482±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
pka
2.52±0.25(Predicted)
InChI
InChI=1S/C8H8N2O4/c1-4-2-3-5(8(11)12)7(6(4)9)10(13)14/h2-3H,9H2,1H3,(H,11,12)
InChIKey
JLWAVVAJFWDXEF-UHFFFAOYSA-N
SMILES
C(O)(=O)C1=CC=C(C)C(N)=C1[N+]([O-])=O
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2-NITRO-3-AMINO-4-METHYLBENZOIC ACID Usage And Synthesis

Synthesis

7356-52-7

37901-90-9

General procedure for the synthesis of 3-amino-4-methyl-2-nitrobenzoic acid from 3-acetamido-4-methyl-2-nitrobenzoic acid: To a solution of 3-acetamido-4-methyl-2-nitrobenzoic acid (79 g, 0.33 mol, 1.0 eq.) in dioxane (400 mL) was added dropwise 6N hydrochloric acid (200 mL). The reaction mixture was heated under reflux conditions overnight. Upon completion of the reaction, it was extracted with ethyl acetate (200 mL × 3). The organic phases were combined and dried over anhydrous sodium sulfate and subsequently concentrated under reduced pressure. The resulting solid was ground with mixed solvents (petroleum ether/ethyl acetate = 10/1, v/v) and filtered to give 3-amino-4-methyl-2-nitrobenzoic acid (60 g, 92.7% yield).

References

[1] Patent: WO2018/218070, 2018, A2. Location in patent: Page/Page column 181; 182
[2] Patent: WO2015/27222, 2015, A2. Location in patent: Paragraph 0279
[3] Patent: WO2007/76092, 2007, A2. Location in patent: Page/Page column 71
[4] Patent: US2004/167194, 2004, A1. Location in patent: Page 23

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