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1-ethyl-3-nitrobenzene

  • Chemical Name: 1-ethyl-3-nitrobenzene
  • CAS: 7369-50-8
  • Purity: 99%
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Factory supply 1-ethyl-3-nitrobenzene 7369-50-8 with low price

  • Molecular Formula: C8H9 N O2
  • Molecular Weight: 151.165
  • Vapor Pressure: 0.0507mmHg at 25°C 
  • Melting Point: -37.9°C 
  • Refractive Index: 1.5359 (estimate) 
  • Boiling Point: 243.2°C at 760 mmHg 
  • Flash Point: 105.3°C 
  • PSA: 45.82000 
  • Density: 1.127g/cm3 
  • LogP: 2.68040 

1-ethyl-3-nitrobenzene(Cas 7369-50-8) Usage

Synthesis Reference(s)

Tetrahedron Letters, 28, p. 1321, 1987 DOI: 10.1016/S0040-4039(00)95359-0

InChI:InChI=1/C8H9NO2/c1-2-7-4-3-5-8(6-7)9(10)11/h3-6H,2H2,1H3

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7369-50-8 Process route

methyl nitrate
598-58-3

methyl nitrate

ethylbenzene
100-41-4,27536-89-6

ethylbenzene

4-ethylnitrobenzene
100-12-9,94234-68-1,34527-20-3

4-ethylnitrobenzene

2-nitro(ethylbenzene)
612-22-6

2-nitro(ethylbenzene)

3-ethylnitrobenzene
7369-50-8

3-ethylnitrobenzene

Conditions
Conditions Yield
Product distribution; gas-phase radiolytic nitration;
ethylbenzene
100-41-4,27536-89-6

ethylbenzene

4-ethylnitrobenzene
100-12-9,94234-68-1,34527-20-3

4-ethylnitrobenzene

2-nitro(ethylbenzene)
612-22-6

2-nitro(ethylbenzene)

3-ethylnitrobenzene
7369-50-8

3-ethylnitrobenzene

Conditions
Conditions Yield
With ortho-methylphenyl iodide; potassium nitrate; sodium nitrite; In trifluoroacetic acid; for 0.5h;
26%
71%
With potassium nitrate; In trifluoroacetic acid; for 0.5h;
48%
49%
With benzoyl nitrate; large port mordenite; In tetrachloromethane; for 1.33333h; Yield given. Yields of byproduct given; Ambient temperature;
With 1-nitro-1H-pyrazole; boron trifluoride diethyl etherate; In dichloromethane; at 25 ℃; for 3h; Title compound not separated from byproducts;
44 % Chromat.
3 % Chromat.
53 % Chromat.
With tetrabutylammonium nitrate; trifluoroacetic anhydride; In chloroform; at 25 ℃;
41.5 % Chromat.
1.7 % Chromat.
56.8 % Chromat.
With Nitrogen dioxide; ozone; In dichloromethane; at -10 ℃; for 3h; Yield given. Yields of byproduct given;
With zeolite BAI-ZSM-5; Nitrogen dioxide; at 80 ℃; Yield given. Yields of byproduct given;
With tetrabutylammonium nitrate; trifluoroacetic anhydride; In acetonitrile; at 25 ℃;
5.9 % Chromat.
44.7 % Chromat.
49.4 % Chromat.
With zeolite ZSM-5-60; Nitrogen dioxide; at 175 ℃; Yield given. Yields of byproduct given;
With silver nitrate; boron trifluoride; In acetonitrile; at 25 ℃; for 5h; Product distribution; competitive nitration benzene, relative rate;
52 % Chromat.
4 % Chromat.
44 % Chromat.
With ammonium cerium(IV) nitrate; In acetonitrile; at 84 ℃; Product distribution; other reagent;
With nitric acid; sulfuric acid; at 75 ℃; Product distribution; other temperature, other solvent, without catalyst;
With Nitrogen dioxide; ozone; In dichloromethane; at 0 ℃; Rate constant; relative rates (competition with benzene), partial rate factors;
With dinitrogen tetraoxide; N,N,N,N-tetraethylammonium tetrafluoroborate; In acetonitrile; at 25 ℃; Product distribution; Variation of solvent. Electrolytic nitration.;
48.2 % Chromat.
4.5 % Chromat.
47.3 % Chromat.
With nitric acid; trifluoroacetic acid; at 25 - 50 ℃; Rate constant; Product distribution; nitration of alkylbenzenes with nitric acid in the system CH3CO2H*H2O; substrate selectivity, electronic and steric effects; effects of temperature and medium composition;
With zeolite BAI-ZSM-5; Nitrogen dioxide; at 125 ℃; Yield given. Yields of byproduct given;
With molecular sieve; nitric acid; acetic anhydride; for 0.166667h; Title compound not separated from byproducts; Ambient temperature;
82 % Chromat.
15 % Chromat.
3 % Chromat.
With nitro acetate; In tetrachloromethane; at -20 - 20 ℃; for 2h; Product distribution; other reagents;
With sulfuric acid; nitric acid; In trifluoroacetic acid; at 25 ℃; Further Variations:; Temperatures; Solvents; pH-values; Product distribution;
With nitric acid; at 100 ℃; for 4h;
With nitric acid; acetic anhydride; In tetrachloromethane;
With poly(4-vinylpyridine)-nitrating mixture complex; In dichloromethane; at 20 ℃; for 1.5h; Overall yield = 96 %; Green chemistry;
With dinitrogen pentoxide; In dichloromethane; at 30 ℃; for 0.0133333h; Flow reactor;

7369-50-8 Upstream products

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7369-50-8 Downstream products

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    m-ethylaniline

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