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Chemical Structure| 500131-50-0 Chemical Structure| 500131-50-0

Structure of 500131-50-0

Chemical Structure| 500131-50-0

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Product Details of [ 500131-50-0 ]

CAS No. :500131-50-0
Formula : C12H17F2N
M.W : 213.27
SMILES Code : CC1=CC(C(F)(F)N(CC)CC)=CC=C1
MDL No. :MFCD12031321
InChI Key :SGDDSVYULWVCQK-UHFFFAOYSA-N
Pubchem ID :11820531

Safety of [ 500131-50-0 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H314
Precautionary Statements:P280-P305+P351+P338-P310
Class:8
UN#:2735
Packing Group:

Application In Synthesis of [ 500131-50-0 ]

* 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 [ 500131-50-0 ]

[ 500131-50-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 4064-06-6 ]
  • [ 500131-50-0 ]
  • [ 2021-97-8 ]
  • [ 134-62-3 ]
  • 2
  • [ 134-62-3 ]
  • [ 500131-50-0 ]
YieldReaction ConditionsOperation in experiment
60% With Carbonyl fluoride; In 1,2-dichloro-ethane; at 158℃; for 10h;Product distribution / selectivity; Example 4: Production of N,N-diethyl-alpha,alpha-difluoro-(3-methyl)benzylamine The same process as in Example 1 was carried out, in which, however, the amount of carbonyl fluoride was changed to 12.5 g (0.19 mol), dichloroethane (50 g) was used as a solvent, and the reaction temperature was changed to 158C. The product was analyzed for NMR, resulting in that the reaction yield of N,N-diethyl-alpha,alpha-difluoro-(3-methyl)benzylamine was 60 % (Table 1).
7 - 62% With Carbonyl fluoride; at 72 - 170℃; for 10h;Product distribution / selectivity; Example 1 Production of N,N-diethyl-alpha,alpha-difluoro-(3-methyl)benzylamine A starting amide compound, N,N-diethyl-metatolamide (19.11 g, 0.1 mol) was put into an autoclave (300 ml), closed and purged with nitrogen. Using a vacuum pump, the autoclave was degassed, and carbonyl fluoride (12.3 g, 0.186 mol) was put into it. With stirring, the contents were heated at 170C with a heater, and reacted at that temperature for 10 hours. After the reaction, the heating was stopped, the pressure in the reactor was reduced, and the unreacted carbonyl fluoride was absorbed by water with ice. In nitrogen, the contents were taken out from the bottom of the reactor and transferred into a flask, the flask was heated at about 60C, and the unreacted carbonyl fluoride was removed under reduced pressure. The product was analyzed for NMR resulting in that the reaction yield of N,N-diethyl-alpha,alpha-difluoro-(3-methyl)benzylamine was 66 %. The product was subjected to distillation under reduced pressure (55 to 57C/4 mmHg), thereby giving an isolated pure substance, N,N-diethyl-alpha,alpha-difluoro-(3-methyl)benzylamine (11.97 g, isolation yield 56 %). The pure product was analyzed for NMR, resulting in that its purity was 100 %. The yield is based on N,N-diethyl-metatolamide (Table 1). (NMR data) 1H-NMR: delta (ppm), TMS standard, in CDCl3, 1.02 (t, 6H, -CH3×2), 2.33 (s, 3H, -CH3), 12.84 (q, 4H, -CH2-×2). 13 C-NMR: delta (ppm), TMS standard, in CDCl3, at -50C, 13.7 (s, -CH3×2), 21.2 (s, -CH3), 40.0 (s, -CH2-×2), 123.7, 127.1, 128.0, 130.6, 137.9 (s, aromatic ring: -CH-×5), 136.2 (t, 32Hz, -CF2). 19 F-NMR: delta (ppm), CF3COOH base, in CDCl3, at -50C, -73.7 (s, =CF2).; Example 3: Production of N,N-diethyl-alpha,alpha-difluoro-(3-methyl)benzylamine The same process as in Example 1 was carried out, in which, however, the amount of carbonyl fluoride was changed to 16.5 g (0.25 mol) and the reaction temperature was to 155c. The product was analyzed for NMR, resulting in that the reaction yield of N,N-diethyl-alpha,alpha-difluoro-(3-methyl)benzylamine was 62 % (Table 1).; Comparative Example 1: Production of N,N-diethyl-alpha,alpha-difluoro-(3-methyl)benzylamine The same process as in Example 1 was carried out, in which, however, the amount of carbonyl fluoride was changed to 12.2 g (0.184 mol) and the reaction temperature was to 120c. The product was analyzed for NMR, resulting in that the reaction yield of N,N-diethyl-alpha,alpha-difluoro-(3-methyl)benzylamine was only 20 % (Table 1).; Comparative Example 3: Production of N,N-diethyl-alpha,alpha-difluoro-(3-methyl)benzylamine The same process as in Example 1 was carried out, in which, however, the amount of N,N-diethyl-metatolamide was changed to 38.51 g (0.2 mol), the amount of carbonyl fluoride was to 17.7 g (0.268 mol) and the reaction temperature was to 72C. The product was analyzed for NMR, resulting in that the reaction yield of N,N-diethyl-alpha,alpha-difluoro-(3-methyl)benzylamine was only 7 % (Table 1).
 

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