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Chemical Structure| 850154-04-0 Chemical Structure| 850154-04-0

Structure of 850154-04-0

Chemical Structure| 850154-04-0

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Product Details of [ 850154-04-0 ]

CAS No. :850154-04-0
Formula : C8H6ClNO3S
M.W : 231.66
SMILES Code : O=S(C1=CC=CC(OC)=C1C#N)(Cl)=O
MDL No. :MFCD18394207

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Application In Synthesis of [ 850154-04-0 ]

* 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 [ 850154-04-0 ]

[ 850154-04-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1591-37-3 ]
  • [ 850154-04-0 ]
YieldReaction ConditionsOperation in experiment
85% 2.2 : 2-Cyano-3-methoxy-phenylsulfonylchloride; 10 g of concentrated hydrochloric acid were slowly added to a solution of 4.0 (27 mmol) of <strong>[1591-37-3]2-amino-6-methoxy-benzonitrile</strong> in 32 ml of glacial acetic acid at room temperature while stirring. The mixture was stirred at room temperatures for 10 minutes. Then a solution of 1.9 g (27.3 mmol) sodium nitrite in 5 mi of water was added at 5-10C and the reaction mixture was stirred at 0C for 1 hour to obtain the diazonium salt. In a separate flask, a saturated solution of sulfur dioxide in 68 ml of glacial acetic acid was prepared at room temperature and a solution of 1.7 g of copper (li) chloride in 4 mi of water was added. The reaction mixture of the diazonium salt which had been prepared beforehand was then quickly added to the solution of the copper salt. The resulting mixture was stirred at room temperature for additional 2.5 hours. The reaction mixture was then poured into ice-cooled water. The aqueous layer was extracted three times with dichloromethane. The combined organic extracts were dried over a drying agent and filtered off with suction. The filtrate was concentrated in vacuo to afford 5.3 g (85% of theory) of the title compound having a melting point of 96-99C.
85% 2.2: 2-Cyano-3-methoxyphenylsulfonyl chloride10 g of concentrated hydrochloric acid were slowly added to a solution of 4.0 g (27 mmol) of <strong>[1591-37-3]2-amino-6-methoxybenzonitrile</strong> in 32 ml of glacial acetic acid at room temperature while stirring. The mixture was stirred at room temperature for 10 minutes. Then, a solution of 1.9 g (27.3 mmol) of sodium nitrite in 5 ml of water was added at 5- 10C and the reaction mixture was stirred at 00C for 1 hour to obtain the diazonium salt. In a separate flask, a saturated solution of sulfur dioxide in 68 ml of glacial acetic acid was prepared at room temperature and a solution of 1.7 g of copper(ll) chloride in 4 ml of water was added. The reaction mixture of the diazonium salt which had been prepared beforehand was then quickly added to the solution of the copper salt. The resulting mixture was stirred at room temperature for an additional 2.5 hours. The reac¬ tion mixture was then poured into ice-cooled water. The aqueous layer was extracted three times with dichloromethane. The combined organic extracts were dried over a drying agent and filtered off with suction. The filtrate was concentrated in vacuo. Yield: 5.3 g (85% of theory) of the title compound having a melting point of 96-99C.
 

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