Basic information Safety Supplier Related

4-(2-METHOXYETHOXY)ANILINE

Basic information Safety Supplier Related

4-(2-METHOXYETHOXY)ANILINE Basic information

Product Name:
4-(2-METHOXYETHOXY)ANILINE
Synonyms:
  • 4-(2-methoxyethoxy)aniline(SALTDATA: HCl)
  • 4-(2-Methoxyethoxy)-benzenaMine
  • p-Phenetidine, β-methoxy-
  • 4-(2-Methoxyethoxy)
  • AKOS BC-2489
  • AKOS BBB/095
  • 4-(2-METHOXYETHOXY)ANILINE
  • ASISCHEM C40525
CAS:
33311-29-4
MF:
C9H13NO2
MW:
167.21
Mol File:
33311-29-4.mol
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4-(2-METHOXYETHOXY)ANILINE Chemical Properties

Boiling point:
142 °C(Press: 3 Torr)
Density 
1.078±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
5.10±0.10(Predicted)
Appearance
Light brown to brown Solid
InChI
InChI=1S/C9H13NO2/c1-11-6-7-12-9-4-2-8(10)3-5-9/h2-5H,6-7,10H2,1H3
InChIKey
DIOBEQCFVVJJBU-UHFFFAOYSA-N
SMILES
C1(N)=CC=C(OCCOC)C=C1
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Safety Information

Hazard Codes 
Xi
HazardClass 
IRRITANT
HS Code 
2922290090
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4-(2-METHOXYETHOXY)ANILINE Usage And Synthesis

Synthesis

22483-40-5

33311-29-4

General procedure for the synthesis of 4-(2-methoxyethoxy)aniline from 4-nitrophenyl-2-methoxyethyl ether: 1-(2-methoxyethoxy)-4-nitrobenzene (38) (3.9 g, 20 mmol), methanol (80 mL), and 10% activated carbon (400 mg) were added to a hydrogenation reactor. The reaction mixture was stirred overnight at room temperature in a hydrogen atmosphere. Upon completion of the reaction, the mixture was filtered through diatomaceous earth to remove the activated carbon. The filtrate was concentrated in vacuum to afford 4-(2-methoxyethoxy)aniline (39) (3.1 g, 93% yield) as a black oily product. m/z (M+1) 168.1 was shown by LC-MS (ESI) analysis.

References

[1] Bioorganic and Medicinal Chemistry Letters, 2016, vol. 26, # 21, p. 5177 - 5181
[2] Patent: CN103864792, 2017, B. Location in patent: Paragraph 0313; 0314; 0315; 0316
[3] Patent: WO2015/131080, 2015, A1. Location in patent: Paragraph 00768; 00770
[4] Patent: WO2014/130693, 2014, A1. Location in patent: Paragraph 00544; 00547
[5] European Journal of Medicinal Chemistry, 1980, vol. 15, # 5, p. 399 - 404

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