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Chemical Structure| 90715-73-4 Chemical Structure| 90715-73-4

Structure of 90715-73-4

Chemical Structure| 90715-73-4

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Product Details of [ 90715-73-4 ]

CAS No. :90715-73-4
Formula : C4H2ClF3O
M.W : 158.51
SMILES Code : C=C(C(F)(F)F)C(Cl)=O
MDL No. :N/A

Safety of [ 90715-73-4 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H314-H226
Precautionary Statements:P210-P280-P370+P378-P303+P361+P353-P304+P340+P310-P305+P351+P338+P310
Class:8(3)
UN#:2920
Packing Group:

Application In Synthesis of [ 90715-73-4 ]

* 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 [ 90715-73-4 ]

[ 90715-73-4 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 381-98-6 ]
  • [ 90715-73-4 ]
YieldReaction ConditionsOperation in experiment
86.6% With Phthaloyl dichloride; at 20 - 135℃; for 2h; In a 200 mL flask was placed 42.0 g (300 millimol) of alpha-(trifluoromethyl) acrylic acid, to which was gradually added 70.0 mL (450 millimol) of phthalic dichloride at room temperature with stirring. Subsequently, by reacting the contents in the flask for 2 hours, while heating in an oil bath at 135C, an orange reaction liquid was obtained. Subsequently, by atmospherically distillating the reaction liquid, 41.2 g (yield rate 86.6%) of colorless transparent product in liquid form was obtained. As a result of analysis for the resultant perfluoro-1-adamantyl acrylate by nuclear magnetic resonance spectra (NMR), there were observed the following absorption. 1H-NMR {270 MHz} : at 6.91 (s, 1H), 7.11 (s, 1H). 13C-NMR {68 MHz} : at 120.91 (quar, JC-F = 273.9 Hz), 135.25 (quar, JC-CF3 = 31.8 Hz), 139.28, 161.92. Thereby, the colorless transparent product was identified asalpha-(trifluoromethyl)acrylic acid chloride.
66% With thionyl chloride; REFERENTIAL EXAMPLE 2 STR14 Thionyl chloride (11.5 ml; 158 mmoles) was added to alpha-trifluoromethylacrylic acid (19.7 g; 141 mmoles), and the mixture was heated under reflux for 22 hours. Distillation of the reaction mixture under atmospheric pressure gave 14.7 g (yield:66%) of alpha-trifluoromethylacryloyl chloride, B.p. 89-90 C. 1 H NMR (CDCl3:TMS): delta6.89(m, 1H), 7.06(m, 1H). 19 F NMR (CDCl3:CFCl3): delta-65.9(bs).
With thionyl chloride; for 0.5h;Heating / reflux; Example 119; N-(4-Cvano-3-trifluoromethyl-phenyl)-2-trifluoromethyl-acrylamide; 2-Trifluoromethyl-acrylic acid (36.0 mmoL) in thionyl chloride (2.86 ml_) was refluxed for 30 min. Excess thionyl chloride was removed in vacuo to yield a residue. 4-Amino-2-trifluoromethyl-benzonitrile (36.0 mmoL) in diethyl ether (50 mL) was added dropwise to the residue at -40C. The reaction mixture was slowly warmed to room temperature. The reaction mixture was then partitioned between diethyl ether and water. The diethyl ether layer was EPO <DP n="151"/>washed with saturated sodium bicarbonate, then brine, dried over anhydrous Na2SO4, filtered and concentrated to yield a brown oil. The crude material (the brown oil) was then purified by column chromatography (silica gel, using ethyl acetate as eluent) to yield the title compound as yellow solid. 1H NMR (CDCI3) delta 8.25 (br, s, 1 H), 7.60 (d, J = 8.0 Hz,1 H), 6.95 (s, 1 H),6.75 (d, J = 8.0 Hz, 1H), 6.25 (s, 1 H), 5.98 (s, 1H).
  • 2
  • [ 381-98-6 ]
  • [ 158140-23-9 ]
  • [ 90715-73-4 ]
YieldReaction ConditionsOperation in experiment
24%; 53% With thionyl chloride; for 5h;Heating / reflux; REFERENCE EXAMPLE 1; Preparation of alpha,alpha,alpha-trifluoromethacrylic acid benzyl esterInto a 500 ml two-necked round-bottomed flask equipped with a condenser and a stirrer, alpha,alpha,alpha-trifluoromethacrylic acid (154.0 g, 1.10 mol) and thionyl chloride (170.1 g, 1.43 mol) were charged and refluxed for 5 hours. By distillation, alpha,alpha,alpha-trifluoromethacrylic acid chloride (92.6 g) having a boiling point of from 88 to 92C, was obtained (yield: 53%). Further, as a byproduct, alpha,alpha,alpha-trifluoromethacrylic acid anhydride (34.0 g) having a boiling point of 106C/31 mmHg was obtained (yield: 24%).
  • 3
  • [ 932-32-1 ]
  • [ 90715-73-4 ]
  • N-(2-chlorophenyl)-N-methyl-2-(trifluoromethyl)acrylamide [ No CAS ]
 

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