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Chemical Structure| 157033-24-4 Chemical Structure| 157033-24-4

Structure of 157033-24-4

Chemical Structure| 157033-24-4

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Product Details of [ 157033-24-4 ]

CAS No. :157033-24-4
Formula : C8H5ClF2O
M.W : 190.57
SMILES Code : O=C(Cl)CC1=CC(F)=CC(F)=C1
MDL No. :MFCD00275597

Safety of [ 157033-24-4 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H314
Precautionary Statements:P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P321-P363-P405-P501
Class:8
UN#:3265
Packing Group:

Application In Synthesis of [ 157033-24-4 ]

* 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 [ 157033-24-4 ]

[ 157033-24-4 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 74-85-1 ]
  • [ 157033-24-4 ]
  • [ 172366-38-0 ]
YieldReaction ConditionsOperation in experiment
88% dissolve 2.1 kg of intermediate II (1 equivalent) in 21 L of dichloroethane,After the dissolution is complete, slowly add 2.6 kg of aluminum trichloride (2 equivalents) to the resulting solution B, stir to dissolve the aluminum trichloride, and then reduce the temperature to below -10 C to obtain the reaction system A. Add sulfuric acid-dried ethylene gas to A, and test while adding ethylene gas, until no intermediate II is detected, stop adding ethylene gas, continue stirring at room temperature overnight, post-treatment to obtain 1.6kg of intermediate III as a tetraketone The structural formula is: In this step, the acid chloride is cyclized with aluminum trichloride in ethylene dichloride and ethylene to form intermediate III, and the reaction yield is 88%.
73.6 g 5,7-Difluoro-2-tetralone. SOCl2 (100 mL) was added in one portion to 3,5-difluorophenylacetic acid (100 g, 0.58 mol) and after stirring for 15 h, the volatiles were evaporated under reduced pressure. The resulting oily acid chloride was dissolved in CH2Cl2 (200 mL) and added dropwise to a mechanically stirred suspension of AlCl3 (154 g, 1.16 mol) in CH2Cl2 (1.0 L). The stirred suspension was cooled to an internal temperature of -65 C in a dry ice/acetone bath, and the acid chloride solution was added at such a rate in order to maintain an internal temperature <-60 C. After the addition was complete, ethylene gas was bubbled through the reaction mixture at a rapid rate for 10 min at -65 C. The reaction mixture was allowed to warm to 0 C over 2 h with stirring, and was then cooled to -10 C and treated with H2O (500 mL) initially dropwise, followed by rapid addition. The organic layer was separated, washed with brine (100 mL) and dried over MgSO4. Evaporation under reduced pressure gave a dark oily residue which was distilled in vacuo on a Kugelrohr collecting material boiling between 90-110 C (1.0 to 0.7 mm Hg). The distillate was redistilled at 100-105 C (0.3 mm Hg) to give the product as a white solid, (73.6 g, 0.40 mol; 70%): mp 46 C; IR (KBr) 1705 cm-1; 1H NMR (CDCl3) δ 2.55 (t, J =7.5 Hz, 2H), 3.10 (t, J = 7.5 Hz, 2H), 3.58 (s, 2H), 6.70 (m, 2H); MS m/z 182 (M+). Anal. Calcd for C10H8F2O: C, 65.93; H, 4.42. Found: C, 65.54; H, 4.42.
  • 2
  • [ 33400-49-6 ]
  • [ 157033-24-4 ]
  • N-{2-amino-6-[(4-fluorobenzyl)amino]pyridin-3-yl}-2-(3,5-difluorophenyl)acetamide [ No CAS ]
 

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