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Chemical Structure| 1262400-04-3 Chemical Structure| 1262400-04-3

Structure of 1262400-04-3

Chemical Structure| 1262400-04-3

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Product Details of [ 1262400-04-3 ]

CAS No. :1262400-04-3
Formula : C6H9F3O3S
M.W : 218.19
SMILES Code : CS(=O)(OCC1(C(F)(F)F)CC1)=O
MDL No. :MFCD28403756

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Application In Synthesis of [ 1262400-04-3 ]

* 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 [ 1262400-04-3 ]

[ 1262400-04-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 124-63-0 ]
  • [ 371917-17-8 ]
  • [ 1262400-04-3 ]
YieldReaction ConditionsOperation in experiment
With triethylamine; In dichloromethane; at 0℃; for 1h; Step 2 (0827) To a solution of (1-(Trifluoromethyl)cyclopropyl)methanol (XXVI) (1.6 g, 11.42 mmol) in DCM (23 mL) was added Et3N (1.9 mL, 13.7 mmol). The reaction was cooled to 0 C. and MsCl was added dropwise. The reaction was stirred at 0 C. for 1 h. The reaction was poured into water, and extracted with DCM. The organic phase was separated, washed with brine, dried, and concentrated. The crude mesylate was then dissolved in acetone (22 mL). LiBr (4.96 g, 57.1 mmol) was added, and the reaction stirred at room temperature overnight. The acetone was carefully removed, and the residue was partitioned between water and ether. The aqueous phase was separated and reextracted with ether. The organic phases were combined, washed with brine, dried, and carefully concentrated to give 1-(bromomethyl)-1-(trifluoromethyl)cyclopropane (XXVII) (1.2867 g, 6.34 mmol, 55.5% yield) as a gold liquid with residual amounts of acetone. 1H NMR (499 MHz, DMSO-d6) δ ppm 1.04 (2H, tquin, J=5.17, 5.17, 1.74, 1.74, 1.74, 1.74 Hz), 1.23-1.27 (2H, m), 3.77 (2H, s).
With triethylamine; In dichloromethane; at 0℃; for 1h; To a solution of <strong>[371917-17-8](1-(trifluoromethyl)cyclopropyl)methanol</strong> (LIX) (1.6 g, 11.42 mmol) in DCM (23 mL) was added Et3N (1.9 mL, 13.7 mmol). The reaction was cooled to 0 C. and MsCl was added dropwise. The reaction was stirred at 0 C. for 1 h. The reaction was poured into water and extracted with DCM. The organic phase was separated, washed with brine, dried, and concentrated. The crude mesylate was then dissolved in acetone (22 mL). LiBr (4.96 g, 57.1 mmol) was added, and the reaction stirred at room temperature overnight. The acetone was carefully removed, and the residue was partitioned between water and ether. The aqueous phase was separated and reextracted with ether. The organic phases were combined, washed with brine, dried, and carefully concentrated to give 1-(bromomethyl)-1-(trifluoromethyl)cyclopropane (LX) (1.2867 g, 6.34 mmol, 55.5% yield) as a gold liquid with residual amounts of acetone. 1H NMR (499 MHz, DMSO-d6) δ ppm 1.04 (2H, tquin, J=5.17, 5.17, 1.74, 1.74, 1.74, 1.74 Hz), 1.23-1.27 (2H, m), 3.77 (2H, s).
 

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