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Chemical Structure| 194018-68-3 Chemical Structure| 194018-68-3

Structure of 194018-68-3

Chemical Structure| 194018-68-3

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Product Details of [ 194018-68-3 ]

CAS No. :194018-68-3
Formula : C9H7F3O5S
M.W : 284.20
SMILES Code : O=S(C(F)(F)F)(OC1=CC=C(C=O)C=C1OC)=O

Safety of [ 194018-68-3 ]

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

Application In Synthesis of [ 194018-68-3 ]

* 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 [ 194018-68-3 ]

[ 194018-68-3 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 194018-68-3 ]
  • [ 21962-49-2 ]
YieldReaction ConditionsOperation in experiment
56% With dicyanozinc;tetrakis(triphenylphosphine) palladium(0); In DMF (N,N-dimethyl-formamide); at 110℃; for 4h; 4-Formyl-2-methoxybenzonitrile [0276] In an oven-dried flask purged with argon, a mixture of sulfonate (880 mg, 3,096 mmol), zinc cyanide (1,454 g, 12,385 mmol) and tetrakis triphenylphosphine palladium (0) (537 mg, 0,464 mmol) in DMF (30 ml) were stirred at 110C for 4h. Et20 was added to the reaction mixture and the organic layer was washed 3 times with water, dried, filtered and concentrated. The crude compound was then purified by flash chromatography (ethyl acetate-hexanes/3: 7) to provide nitrile (280 mg, 56%). 1H RMN (400 MHz, acetone d6) 8 : 4.11 (s, 3H), 7.68 (dd, 1H, J= 1.2 and 7.7 Hz), 7.72 (d, lH, J= 1. 2 Hz), 7.95 (d, 1H, J= 7.7 Hz), 10.14 (s, 1H),
  • 2
  • [ 557-21-1 ]
  • [ 194018-68-3 ]
  • [ 21962-49-2 ]
YieldReaction ConditionsOperation in experiment
tetrakis(triphenylphosphine) palladium(0); In N,N-dimethyl-formamide; at 110℃; for 8h; A mixture of 4-formyl-2-methoxyphenyl trifluoromethanesulfonate (37.0 g, 130 mmol), zinc cyanide (61.0 g, 521 mmol) and tetrakis triphenylphosphine palladium (0) (22.6 g, 19.5 mmol) in DMF (300 mL) were stirred at 110 0C for 8 h. EtOAc was added to the reaction mixture and the organic layer was washed two times with water, dried, filtered and concentrated. The crude product was then purified by column chromatography (silica gel, ethylacetate/hexanes 3:7) which afforded 4-formyl-2-methoxybenzonitrile.1H NMR (CDCl3, 500 MHz) δ 10.08 (s, IH), 7.80 (d, J= 7.5 Hz, IH), 7.55 (d, J= 7.5 Hz. IH),7.51 (s, IH), 4.06 (s, 3H); LC/MS (IE, m/z) 162.07 [M + I]+.
With tetrakis(triphenylphosphine) palladium(0); In N,N-dimethyl-formamide; at 110℃; for 8h; Step B: 4-Formyl-2-methoxybenzonitrile: A mixture ofthe sulfonate (37.0 g, 130 mmol), zinc cyanide (61.1 g, 521 mmol) and tetrakis triphenylphosphine palladium (0) (22.57 g, 19.53 mmol)in DMF (300 mL) were stirred at 110 C for 8 hr. EtOAc was added to the reaction mixture andthe organic layer was washed two times with water, dried, filtered and concentrated. The crudeproduct was then purified by column chromatography (silica gel, ethylacetate/hexanes 3:7) whichafforded the title compound: LC/MS: (IE, mlz) [M + 1 t = 162.34.
  • 3
  • [ 748101-41-9 ]
  • [ 194018-68-3 ]
  • [ 21962-49-2 ]
YieldReaction ConditionsOperation in experiment
With tetrakis(triphenylphosphine) palladium(0); In N,N-dimethyl-formamide; at 110℃; for 8h; A mixture of 4-formyl-2-methoxyphenyltrifluoromethanesulfonate (37.0 g, 130 mmol), zinc cyanide (6 1.0 g, 521 mmol) and tetrakistriphenylphosphine palladium (0) (22.6 g, 19.5 mmol) in DME (300 mL) were stirred at 110 c for 8 h. EtOAc was added to the reaction mixture and the organie layer was washed two times with water, dried, filtered and concentrated. The crude product was then purified by column chromatography (silica gel, ethylacetatelhexanes 3:7) which afforded 4-formyl-2-methoxybenzonitrile._Lc/MS (IE, miz) 162.07 [M + 11+.
With tetrakis(triphenylphosphine) palladium(0); In N,N-dimethyl-formamide; at 110℃; for 8h; General procedure: A mixture of the sulfonate (37.0 g, 130 mmol), zinc cyanide (61.1 g, 521mmol) and tetrakis triphenylphosphine palladium (0) (22.57 g, 19.53 mmol) in DMF (300 mL) were stirred at 110 Cfor 8 hr. EtOAc was added to the reaction mixture and the organic layer was washed two times with water, dried,filtered and concentrated. The crude product was then purified by column chromatography (silica gel, ethylacetate/hexanes 3:7) which afforded the title compound: LC/MS: (IE, m/z) [M + 1]+ = 162.34.
  • 4
  • zinc cyanide [ No CAS ]
  • [ 194018-68-3 ]
  • [ 21962-49-2 ]
YieldReaction ConditionsOperation in experiment
With tetrakis(triphenylphosphine) palladium(0); In N,N-dimethyl-formamide; at 110℃; for 8h; A mixture of 4-formyl-2-methoxyphenyl trifluoromethanesulfonate (37.0 g, 130 mmol), zinc cyanide (61.0 g, 521 mmol) and tetrakis triphenylphosphine palladium (0) (22.6 g, 19.5 mmol) in DMF (300 mL) was stirred at 110C for 8 h. EtOAc was added to the reaction mixture and the organic layer was washed two times with water, dried, filtered and concentrated. The crude product was then purified by column chromatography eluting with 30% EtOAc/hexanes, which afforded 4-formyl-2- methoxybenzonitrile. LC/MS: [(M+l)]+ = 162.
  • 5
  • [ 80041-89-0 ]
  • [ 194018-68-3 ]
  • [ 71745-73-8 ]
 

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