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Chemical Structure| 80058-85-1 Chemical Structure| 80058-85-1

Structure of 80058-85-1

Chemical Structure| 80058-85-1

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Product Details of [ 80058-85-1 ]

CAS No. :80058-85-1
Formula : C18H23NO
M.W : 269.38
SMILES Code : NC1=C(C(C)C)C=C(OC2=CC=CC=C2)C=C1C(C)C
MDL No. :MFCD09835410
InChI Key :WRBGLNGTYOVAJO-UHFFFAOYSA-N
Pubchem ID :13272139

Safety of [ 80058-85-1 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H312-H315-H319-H332-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 80058-85-1 ]

* 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.

  • Downstream synthetic route of [ 80058-85-1 ]

[ 80058-85-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 80058-84-0 ]
  • [ 108-95-2 ]
  • [ 80058-85-1 ]
YieldReaction ConditionsOperation in experiment
94 - 99% With potassium carbonate;1-methyl-1H-imidazole; copper(l) chloride; In o-xylene; at 120 - 140℃; for 30h;Heating / reflux;Product distribution / selectivity; To 32.4 g (0.234 mol) K2CO3, 0.58 g (5.8 mmol) CuCl, 13.2 g (0.14 mol) phenol, and 30 g (0.117 mol) 4-bromo-2,6-di-iso-propylaniline 2 in a 250 mL three-necked bulb with argon inlet, reflux condenser and stopper 4.7 mL (58 mmol) 1-methylimidazole and 100 mL o-xylene were added under argon atmosphere. The mixture was stirred and heated to 140° C., until thin layer chromatography (eluent toluene) showed no residual starting material 4-bromo-2,6-di-iso-propylaniline (ca. 30 h). After cooling, water and diethyl ether were added, the organic phase was washed with 10percent K2CO3 solution, water and brine and dried over Na2SO4. After evaporation of the solvents, an aliquot part of the dark oily material was filtered through a short silica gel plug with toluene as solvent to give, after removal of the solvent and drying in vacuum, a dark solid. The purity is determined to 95percent by gc, The calculated yield is 99percentMS (m/z, (intensity)): 269 (100), 254 (97), 146 (10), 134 (7), 77 (10).1H (CDCl3. 400 MHz, 300K): 7.27 (m, 2H); 6.99 (m, 1H); 6.92 (m, 2H); 6.77 (s, 2H); 3.62 (bs, 2H, NH2); 2.94 (hept., 2H, CH(CH3)2); 1.24 (d, 12H, CH(CH3)2). 13C (CDCl3. 100 MHz, 300K): 159.21; 148.30; 136.57; 134.32; 129.45; 121.61; 116.75; 115.08; 28.14; 22.39.
With potassium hydroxide; potassium carbonate; In basic copper carbonate powder; N,N-dimethyl-formamide; toluene; With stirring, 21 g (0.15 mol) of potassium carbonate are initially added to 141 g (1.5 mol) of phenol in 500 g of toluene, followed by the addition of 168 g (1.5 mol) of a 50percent aqueous solution of potassium hydroxide. The entire water of reaction is then separated under reflux, and then ca. 400 g of toluene are removed by distillation. The residue is dissolved in 700 g of dimethyl formamide. After addition of 6 g (0.05 mol) of copper carbonate, solvent is distilled off until the temperature of the reaction mixture is 140° C. Then 256 g (1 mol) of <strong>[80058-84-0]4-bromo-2,6-diisopropylaniline</strong> are added at 140° C. and the mixture is kept for 10 hours at 140° C. The dimethyl formamide is then removed by vacuum distillation, the residue is extracted with water, and the product is taken up in toluene. After stripping off the toluene, the crude product is purified by vacuum distillation, giving 215 g (80percent of theory) of 4-phenoxy-2,6-diisopropylaniline with a boiling point of 142°-145° C./0.04 mbar and a melting point of 69°-71° C., in the form of a bright red product.
With potassium hydroxide;copper chloride; In 5,5-dimethyl-1,3-cyclohexadiene; (a) Production of 2,6-diisopropyl-4-phenoxyaniline 48.9 g of phenol are dissolved in 500 ml of xylene, and to this solution are added 30.2 g of pulverised potassium hydroxide in an atmosphere of nitrogen. The reaction mixture is stirred and heated to boiling point, while continuously distilling off the water that is formed. After addition of 0.6 g of copper chloride and 100 g of <strong>[80058-84-0]2,6-diisopropyl-4-bromoaniline</strong>, the mixture is stirred for 8 hours at 150°-155° C., then cooled, and filtered with suction. The filtrate is washed with 15percent sodium hydroxide solution (150 ml) and with two 150 ml portions of water. The organic phase is separated and dried over sodium sulfate. The solvent is removed by distillation and the product is distilled, affording the compound of the formula STR5 with a boiling point of 103°-104° C./0.01 torr and a melting point of 71°-72° C. (after recrystallisation from hexane). The following anilines are also obtained in analogous manner: STR6
 

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