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Chemical Structure| 1231755-15-9 Chemical Structure| 1231755-15-9

Structure of 1231755-15-9

Chemical Structure| 1231755-15-9

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Product Details of [ 1231755-15-9 ]

CAS No. :1231755-15-9
Formula : C9H15F3N2O3
M.W : 256.22
SMILES Code : O=C(NCC(NCC(F)(F)F)=O)OC(C)(C)C
MDL No. :MFCD24391841

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Application In Synthesis of [ 1231755-15-9 ]

* 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 [ 1231755-15-9 ]

[ 1231755-15-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1231755-15-9 ]
  • [ 1171331-39-7 ]
YieldReaction ConditionsOperation in experiment
100% With hydrogenchloride; In methanol; at 20℃; for 12h; 2-/V-(te/f-Butoxycarbonyl)-1 -oxo-1-N-(2,2,2-trifluoroethyl)-1 ,2-diaminoethane (1 eq) was dissolved in 2M HCI/MeOH and stirred for 12 h at room temperature. The reaction mixture was concentrated under reduced pressure till dryness to afford the title compound in quantitative yield.
66% With hydrogenchloride; In ethyl acetate; at 18 - 35.5℃;Product distribution / selectivity; A portion of the product of Example 2, Step A (11.7 g) was diluted with ethyl acetate (50 mL) and treated with hydrogen chloride gas at 18-35.5 C until the starting material was consumed. The resulting slurry was cooled to 0-5 C, stirred for approximately 1 hour at that temperature, and then filtered. The residue was washed twice with ethyl acetate (20 ml each) and dried in a vacuum oven at 60C to give the title compound as a white solid (7.22 g, 66% yield).1H NMR (DMSO-d6): 9.24 (tr, / = 6.2 Hz, 1H), 8.3 (s, 3H), 4.11-3.89 (m, 2H), 3.64 (s, 2H), 1.21-1.50 ppm (s, 9H); 19F-NMR (DMSO-d6): -70.69 ppm (tr, / = 10.1Hz).
2.4 g With hydrogenchloride; In 1,4-dioxane; at 0 - 24℃; for 10h; Example 95 Preparation of 2-amino-N-(2,2,2-trifluoroethyl)acetamide hydrochloride (C350) To a stirred solution of tert-butyl (2-oxo-2-((2,2,2-trifluoroethyl)amino)ethyl)carbamate (C362; 3 g, 15.6 mmol) in dioxane (20 mL) was added 4 M HCl in dioxane (23 mL, 93.8 mmol) dropwise at 0 C., and the reaction mixture was stirred at room temperature for 10 hours. The reaction mixture was concentrated under reduced pressure. The title compound was isolated as an off-white solid (2.4 g), which was used without purification: 1H NMR (300 MHz, DMSO-d6) delta 9.17-9.13 (m, 1H), 8.21 (br s, 3H), 4.07-3.95 (m, 2H), 3.67-3.64 (m, 2H).
 

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