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2,6-Dichloro-3,5-dimethoxyaniline

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2,6-Dichloro-3,5-dimethoxyaniline Basic information

Product Name:
2,6-Dichloro-3,5-dimethoxyaniline
Synonyms:
  • 2,6-Dichloro-3,5-dimethoxyaniline
  • 2,6-Dichloro-3,5-dimethoxybenzenamine
  • Benzenamine, 2,6-dichloro-3,5-dimethoxy-
  • 2,6-Dichloro-3,5-dimethoxy-phenylamine
  • 157427
  • oro-3,5-dimethoxyaniL
CAS:
872509-56-3
MF:
C8H9Cl2NO2
MW:
222.07
Mol File:
872509-56-3.mol
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2,6-Dichloro-3,5-dimethoxyaniline Chemical Properties

Boiling point:
320℃
Density 
1.357
Flash point:
147℃
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
pka
-0.13±0.10(Predicted)
Appearance
White to off-white Solid
InChI
InChI=1S/C8H9Cl2NO2/c1-12-4-3-5(13-2)7(10)8(11)6(4)9/h3H,11H2,1-2H3
InChIKey
LCQFHEIDCMPNAN-UHFFFAOYSA-N
SMILES
C1(N)=C(Cl)C(OC)=CC(OC)=C1Cl
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Safety Information

HS Code 
2922299090
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2,6-Dichloro-3,5-dimethoxyaniline Usage And Synthesis

Chemical Properties

White to off-white powder

Uses

2,6-Dichloro-3,5-dimethoxyaniline is primarily used as an intermediate in the synthesis of pharmaceuticals.

Synthesis

943189-21-7

872509-56-3

N-(2,6-dichloro-3,5-dimethoxyphenyl)acetamide (34.5 g, 131 mmol) was used as a raw material and dissolved in ethanol (600 mL). Subsequently, 2N aqueous potassium hydroxide solution (400 mL) was added to this solution to obtain the reaction mixture. The reaction mixture was heated to 90°C and stirred, and the reaction was kept at reflux for 2 days. Upon completion of the reaction, the mixture was cooled to room temperature, then cooled to 0 °C in an ice water bath and stirring was continued for 1 hour. The precipitated solid was collected by filtration, washed with cold ethanol/water (1:1, v/v) mixed solvent and dried to give 2,6-dichloro-3,5-dimethoxyaniline (22.1 g, 76% yield). The product was characterized by 1H NMR (400 MHz, DMSO-d5): δ 6.21 (s, 1H), 5.40 (s, 2H), 3.83 (s, 6H).

References

[1] Journal of Medicinal Chemistry, 2011, vol. 54, # 20, p. 7066 - 7083
[2] Patent: US2016/145240, 2016, A1. Location in patent: Paragraph 0098; 0099
[3] Patent: WO2016/164703, 2016, A1. Location in patent: Page/Page column 36
[4] Patent: WO2016/164754, 2016, A1. Location in patent: Page/Page column 33
[5] Patent: WO2006/420, 2006, A1. Location in patent: Page/Page column 157

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