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Chemical Structure| 1443684-70-5 Chemical Structure| 1443684-70-5

Structure of 1443684-70-5

Chemical Structure| 1443684-70-5

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Product Details of [ 1443684-70-5 ]

CAS No. :1443684-70-5
Formula : C7H3ClF4O3S
M.W : 278.60
SMILES Code : O=S(C(F)(F)F)(OC1=C(F)C=CC=C1Cl)=O
MDL No. :MFCD25541813

Safety of [ 1443684-70-5 ]

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

Application In Synthesis of [ 1443684-70-5 ]

* 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 [ 1443684-70-5 ]

[ 1443684-70-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 2040-90-6 ]
  • [ 1025373-45-8 ]
  • [ 1443684-70-5 ]
YieldReaction ConditionsOperation in experiment
With pyridine; In dichloromethane; at 0 - 20℃; for 3h; To a stirred solution of pyridine (26.7 mL, 207 mmol, 1 eq) and <strong>[2040-90-6]2-chloro-6-fluorophenol</strong> (30.3 g, 207 mmol, 1 eq) in methylene chloride (380 mL) at 0° C. was added trifluoromethanesulfonic anhydride (45.2 mL, 207 mmol, 1 eq) dropwise. The mixture was stirred at RT for 3 hrs, evaporated, dissolved in EtOAc, washed with water and brine, dried over anhydrous magnesium sulfate, filtered and evaporated to yield 2-chloro-6-fluorophenyl trifluoromethanesulfonate as a yellow oil that was used without purification.
With pyridine; In dichloromethane; at 0 - 20℃; To a stirred solution of pyridine (26.7 mL, 207 mmol, 1 eq) and <strong>[2040-90-6]2-chloro-6-fluorophenol</strong> (30.3 g, 207 mmol, 1 eq) in methylene chloride (380 mL) at 0° C. was added trifluoromethanesulfonic anhydride (45.2 mL, 207 mmol, 1 eq) dropwise. The mixture was stirred at RT for 3 hrs, evaporated, dissolved in EtOAc, washed with water and brine, dried over anhydrous magnesium sulfate, filtered and evaporated to yield 2-chloro-6-fluorophenyl trifluoromethanesulfonate as a yellow oil that was used without purification.
  • 2
  • [ 358-23-6 ]
  • [ 2040-90-6 ]
  • [ 1443684-70-5 ]
YieldReaction ConditionsOperation in experiment
100% With pyridine; at 0 - 20℃; To a stirred solution o ophenol (5.00 g, 34.1) in pyridine (100 mL) at 0 °C was added dropwise (trifluoromethane)sulfonyl trifluoromethanesulfonate (19.3 g, 68.4 mmol) dropwise. The mixture was allowed to warm to room temperature and was stirred overnight. The reaction mixture was concentrated and the residue was partitioned between ethyl acetate and water. The organic layer was washed with brine, dried (Na2SO4) and concentrated to afford 2-chloro-6-fluorophenyl trifluoromethanesulfonate (9.5 g, 100percent) as a brown liquid.
With pyridine; In dichloromethane; at 0 - 20℃; for 3h; To a stirred solution of pyridine (26.7 mL, 207 mmol, 1 eq) and <strong>[2040-90-6]2-chloro-6-fluorophenol</strong> (30.3 g, 207 mmol, 1 eq) in methylene chloride (380 mL) at 0° C. was added trifluoromethanesulfonic anhydride (45.2 mL, 207 mmol, 1 eq) dropwise. The mixture was stirred at RT for 3 hrs, evaporated, dissolved in EtOAc, washed with water and brine, dried over anhydrous magnesium sulfate, filtered and evaporated to yield 2-chloro-6-fluorophenyl trifluoromethanesulfonate as a yellow oil that was used without purification.
With pyridine; In dichloromethane; at 0℃; for 3h; To the solution of 2-chloro-6-fiuorophenol (800 mg, 5.46 mmoi) in 10 mL DCM at 0 "C was added pyridine (442 pL 5.48 mmoi) and frifluoromethanesulfonic acid anhydride (918 mu, 5.45 mmoi). The reaction was stirred at the same temperature for 3h. The completion of the reaction was monitored by HPLG. Upon completion, solvent was evaporated in vacuo, H2Q was added to the crude residue and the reaction mixture was extracted with EtOAc. The combined organic layers were washed with brine and dried over NazS04, Filtration and removal of the solvent provided 1 ,25 g of the title compound as a colorless solid, which was used without Further purification; 1H NMR (400 MHz, COCI3) delta = 7.34 ~ 7.31 (m, 2 H);, 7.24 - 7.18 (m, 1 H).
 

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