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Chemical Structure| 773874-76-3 Chemical Structure| 773874-76-3

Structure of 773874-76-3

Chemical Structure| 773874-76-3

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Product Details of [ 773874-76-3 ]

CAS No. :773874-76-3
Formula : C10H12ClNO2
M.W : 213.66
SMILES Code : O=C(OC)C1=CC=C(N(C)C)C=C1Cl
MDL No. :MFCD06203951

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Application In Synthesis of [ 773874-76-3 ]

* 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 [ 773874-76-3 ]

[ 773874-76-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 506-59-2 ]
  • [ 67-68-5 ]
  • [ 85953-29-3 ]
  • [ 773874-76-3 ]
YieldReaction ConditionsOperation in experiment
99% With potassium carbonate; a) 2-Chloro-4-dimethylamino-benzoic acid methyl ester (1a) To a stirred solution of 4,00g (20.6 mmol) <strong>[85953-29-3]2-chloro-4-fluoro-benzoic acid methyl ester</strong> (Apollo) and 60 ml dimethylsulphoxid are added 2.03 g (24,7 mmol) dimethylamine hydrochloride and 5,97 g (43.2 mmol) potassium carbonate. The reaction mixture is stirred over night and is reduced with high vacuum rotation evaporator at 65C. The residue is diluted with dichloromethane, washed twice with water. The combined water phases are extracted with dichloromethane. The combined dichloromethane phases are washed with diluted sodium hydrogen carbonate solution, dried with sodium sulphate and concentrated. The oily crude product 1a is obtained in 99% yield (4,36 g, 20.4 mmol) and is used for the next step without purification. MS-ESI: 213/215 (M+ +1, 64/48).
  • 2
  • [ 506-59-2 ]
  • [ 85953-29-3 ]
  • [ 773874-76-3 ]
YieldReaction ConditionsOperation in experiment
99% With potassium carbonate; In dimethyl sulfoxide; To a stirred solution of 4,00g (20.6 mmol) <strong>[85953-29-3]2-chloro-4-fluoro-benzoic acid methyl ester</strong> (Apollo) and 60 ml dimethylsulphoxid are added 2.03 g (24,7 mmol) dimethylamine hydrochloride and 5,97 g (43.2 mmol) potassium carbonate. The reaction mixture is stirred over night and is reduced with high vacuum rotation evaporator at 65C. The residue is diluted with dichloromethane, washed twice with water. The combined water phases are extracted with dichloromethane. The combined dichloromethane phases are washed with diluted sodium hydrogen carbonate solution, dried with sodium sulphate and concentrated. The oily crude product 2.3.3.a is obtained in 99% yield (4,36 g, 20.4 mmol) and is used for the next step without purification. MS-ESI: 213/215 (M+ +1, 64 / 48). Elementary analysis: Calculated: C 56.21% H 5.66% N 6.56% Determined: C 56.39% H 5,67% N 6.54%
99% With potassium carbonate; In dimethyl sulfoxide; Example 1a) 2-Chloro-4-dimethylamino-benzoic acid methyl ester (1a)To a stirred solution of 4,0Og (20.6 mmol) <strong>[85953-29-3]2-chloro-4-fluoro-benzoic acid methyl ester</strong> (Apollo) and 60 ml dimethylsulphoxid were added 2.03 g (24,7 mmol) dimethylamine hydrochloride and 5,97 g (43.2 mmol) potassium carbonate. The reaction mixture was stirred over night and is reduced with high vacuum rotation evaporator at 65C. The residue was diluted with dichloromethane, washed twice with water. The combined water phases were extracted with dichloromethane. The combined dichloromethane phases were washed with diluted sodium hydrogen carbonate solution, dried with sodium sulphate and concentrated. The oily crude product 1a was obtained in 99 % yield (4,36 g,20.4 mmol) and was used for the next step without purification.MS-ESI: 213 / 215 (M+ +1 , 64 / 48). Elementary analysis:Calculated: C 56.21% H 5.66% N 6.56% Determined: C 56.39% H 5,67% N 6.54%
 

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