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Chemical Structure| 56734-11-3 Chemical Structure| 56734-11-3

Structure of 56734-11-3

Chemical Structure| 56734-11-3

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Product Details of [ 56734-11-3 ]

CAS No. :56734-11-3
Formula : C11H10N2O2S
M.W : 234.27
SMILES Code : O=S(C1=NC=CC(C2=CC=CC=C2)=N1)(C)=O
MDL No. :MFCD06496101

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Application In Synthesis of [ 56734-11-3 ]

* 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 [ 56734-11-3 ]

[ 56734-11-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 56734-10-2 ]
  • [ 56734-11-3 ]
YieldReaction ConditionsOperation in experiment
With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; To a solution of <strong>[56734-10-2]2-methylthio-4-phenylpyrimidine</strong> (0.76 g) in dichloromethane (15 ml) at 0 C. was added portionwise over 15 minutes meta-chloroperbenzoic acid (1.65 g). The resulting white emulsion was warmed to room temperature and stirred for a further 3% hours. The reaction mixture was evaporated to give a white solid. The solid was redissolved in dichloromethane and washed with saturated aqueous sodium bicarbonate solution (*2), and then with water (*2). The resulting solution was dried, filtered and evaporated to give crude 2-methanesulphonyl-4-phenylpyrimidine (0.84 g) as a yellowish solid which was used in the next stage without further purification.
In hexane; dichloromethane; 3-chloro-benzenecarboperoxoic acid; EXAMPLE 68 2-Methylsulfonyl-4-phenylpyrimidine A solution of 2.02 g. of <strong>[56734-10-2]2-methylthio-4-phenylpyrimidine</strong> in 50 ml. of methylene chloride is cooled in an ice bath with 4.33 g. of m-chloroperbenzoic acid being added portionwise. After standing at room temperature overnight, the reaction mixture is washed with a saturated potassium carbonate solution, separated, and dried over anhydrous sodium sulfate. The solution is passed through a short pad of hydrous magnesium silicate absorbent and the eluent is refluxed on a steam bath with addition of hexane until crystallization is induced. On cooling the desired compound is removed by filtration, m.p. 135.5-137 C. Rec. Trav. Chim. 93, 375 (1974), m.p. 135-135.5 C.
 

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