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Chemical Structure| 618-86-0 Chemical Structure| 618-86-0

Structure of 618-86-0

Chemical Structure| 618-86-0

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Product Details of [ 618-86-0 ]

CAS No. :618-86-0
Formula : C6H3ClN2O4
M.W : 202.55
SMILES Code : O=[N+](C1=CC([N+]([O-])=O)=CC(Cl)=C1)[O-]
MDL No. :MFCD11106349

Safety of [ 618-86-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 618-86-0 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Upstream synthesis route of [ 618-86-0 ]
  • Downstream synthetic route of [ 618-86-0 ]

[ 618-86-0 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 618-86-0 ]
  • [ 5344-44-5 ]
YieldReaction ConditionsOperation in experiment
84% With diammonium sulfide In ethanol; water for 1 h; Heating / reflux The above product (0.50 g, 2.47 mmol) was refluxed 1 hr in 6 mL alcohol and 3 mL 20percent ammonium sulfide in H2O. Water was added and the product was filtered, dried and flash chromatographed on silica gel eluting with 10percent acetone-pet ether to obtain 3-chloro-5-nitroaniline (0.36 g, 84percent) as an orange powder.
53% With diammonium sulfide In ethanol; water at 80℃; for 1 h; Example 883-Chloro-5-nitroaniline1-Chloro-3,5-dinitrobenzene (512 mg, 2.5 mmol) was dissolved into EtOH (8 ml) with the aid of sonication. (NH4)2S (3 ml, 20percent in H2O) was added to the solution and heated at 80° C. for 1 hour, followed by thin layer chromatography (3:1 Hexanes:Ethyl Acetate). After the completion of reaction, the solution was allowed to cool to room temperature, ethyl acetate (75 ml) was added and washed with brine (30 ml). The 2 layers were separated, the organic layer was dried with Na2SO4 and concentrated under reduced pressure after filtering off solid. The title compound (225 mg, 53percent yield) was obtained by purifying the residue with flash column chromatography (3:1 Hexanes:Ethyl Acetate) as an orange solid.1H NMR (300 MHz, DMSO) δ 7.32 (s, 1H), 7.24 (s, 1H), 6.94 (s, 1H), 6.14 (s, 2H); LCMS (m/z): 173.04 (MH+).
28% With diammonium sulfide; water In ethanol at 80℃; for 1 h; To a stirred solution of 1-chloro-3,5-dinitrobenzene 8 (3.80 g, 19 mmol) in ethanol (60 mL) was added ammonium sulfide (20percent aqueous solution, 20 mL) and the mixture was heated at 80°C for lh. The mixture was then partitioned between water and ethyl acetate, the ethyl acetate layer was dried over anhydrous sodium sulfate, filtered and solvents evaporated to obtain a crude material, purification of which by flash chromatography on silica gel (using 40 g SNAP column and 30percent ethyl acetate in hexane as eluent) afforded 3-chloro-5-nitroaniline precursor-Olin 28percent yield as orange colored solid. MS: 171.02 (M+H).
References: [1] Patent: US6353013, 2002, B1, . Location in patent: Page column 28.
[2] Patent: US2011/130415, 2011, A1, . Location in patent: Page/Page column 65.
[3] Patent: WO2015/25197, 2015, A1, . Location in patent: Paragraph 00070.
[4] Journal of the Chemical Society, 1905, vol. 87, p. 1265.
[5] Bulletin de la Societe Chimique de France, 1938, vol. <5> 5, p. 1441,1444[6] Anales de la Asociacion Quimica Argentina (1921-2001), 1938, vol. 26, p. 41,44, 45.
[7] Journal of Organic Chemistry, 1975, vol. 40, # 20, p. 2906 - 2910.
[8] Journal of Organic Chemistry, 1977, vol. 42, # 1, p. 166 - 169.
[9] Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1974, p. 1860 - 1862.
[10] Angewandte Chemie - International Edition, 2009, vol. 48, # 50, p. 9538 - 9541.
[11] Journal of Agricultural and Food Chemistry, 2016, vol. 64, # 18, p. 3697 - 3704.
 

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