4-Ethyl-3-nitroaniline

4-Ethyl-3-nitroaniline Suppliers list
Company Name: Beijing Taiya Jie Technology Development Co., Ltd.  
Tel: 021-33690831-8001 13552411790;18616022633
Email: postmaster@tyjchem.cn
Company Name: Bide Pharmatech Ltd.  
Tel: 400-164-7117 18317119277
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Company Name: Nanjing Duolong Bio-tech Co.,Ltd.  
Tel: 18905173768
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Company Name: Shanghai ZhengXia Medical Technology Co., Ltd.  
Tel: 13585673075
Email: 317388297@qq.com
Company Name: Quzhou AMK BioTech Co., Ltd  
Tel: 0570-3081766 18357083060
Email: sales@qzamkbio.com

4-Ethyl-3-nitroaniline manufacturers

4-Ethyl-3-nitroaniline Basic information
Product Name:4-Ethyl-3-nitroaniline
Synonyms:4-ethyl-3-nitrobenzeneamine;3-Nitro-4-ethylaniline;Benzenamine, 4-ethyl-3-nitro-;4-Ethyl-3-nitroaniline 4-ethyl-3-nitroaniline;4-Ethyl-3-nitroaniline
CAS:51529-96-5
MF:C8H10N2O2
MW:166.18
EINECS:
Product Categories:
Mol File:51529-96-5.mol
4-Ethyl-3-nitroaniline Structure
4-Ethyl-3-nitroaniline Chemical Properties
Melting point 44-45 °C
Boiling point 305.7±22.0 °C(Predicted)
density 1.218±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka2.90±0.10(Predicted)
AppearanceLight yellow to yellow Solid
Safety Information
HS Code 2921490090
MSDS Information
4-Ethyl-3-nitroaniline Usage And Synthesis
Synthesis
4-Ethylaniline

589-16-2

4-ETHYL-3-NITROANILINE

51529-96-5

Step 1: 4-Ethylaniline (10.3 mL, 82.5 mmol) was slowly added dropwise to 96% sulfuric acid (63 mL), and the reaction system was cooled to 8°C and ensured that the temperature was maintained below 10°C. After the dropwise addition was completed, the reaction mixture was further cooled to -5 °C, followed by the slow addition of a mixed acid consisting of 100% nitric acid (4 mL) and 96% sulfuric acid (10 mL), controlling the reaction temperature below 0 °C. The reaction mixture was stirred continuously at -5°C for 1 hour. Upon completion of the reaction, the mixture was slowly poured into ice water (200 mL), precipitated, filtered and washed with water. The resulting solid was resuspended in water (100 mL) and neutralized to neutral with 35% ammonium hydroxide solution. The precipitate was collected by filtration and dried in an oven to give the light brown solid product 4-ethyl-3-nitroaniline (10 g, 73% yield). The product was characterized by 1H NMR (400 MHz, DMSO-d6): δ 1.11 (t, J = 7.45 Hz, 3H), 2.63 (q, J = 7.45 Hz, 2H), 5.53 (s, 2H), 6.81 (dd, J = 8.30, 2.44 Hz, 1H), 7.04 (d, J = 2.44 Hz, 1H), 7.11 ( d, J = 8.30 Hz, 1H).

References[1] Patent: WO2012/139930, 2012, A1. Location in patent: Page/Page column 72
[2] Patent: WO2012/143248, 2012, A1. Location in patent: Page/Page column 23
[3] Patent: WO2014/19908, 2014, A2. Location in patent: Page/Page column 32
[4] Patent: US2014/51708, 2014, A1. Location in patent: Paragraph 0717-0719
[5] Journal of the Chemical Society, 1930, p. 252,255
4-Ethyl-3-nitroaniline Preparation Products And Raw materials
Raw materials4-Ethylaniline-->Ammonium hydroxide
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