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Chemical Structure| 35991-61-8 Chemical Structure| 35991-61-8

Structure of 35991-61-8

Chemical Structure| 35991-61-8

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Product Details of [ 35991-61-8 ]

CAS No. :35991-61-8
Formula : C12H12S3
M.W : 252.42
SMILES Code : C12=C(CCS3)C3=C(CCS4)C4=C1CCS2

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Application In Synthesis of [ 35991-61-8 ]

* 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 [ 35991-61-8 ]

[ 35991-61-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 35991-61-8 ]
  • [ 29150-63-8 ]
YieldReaction ConditionsOperation in experiment
51% With chloranil; In toluene; for 48h;Reflux; General procedure: Chloranil and dihydrothiophene derivative were refluxed in toluene. After completion of the reaction (monitored by TLC), the excess of chloranil was removed by mean of vacuum filtration. Then the filtrate was concentrated under reduced pressure to provide the crude product which was subsequently purified by column chromatography (silica gel; hexane as eluent) to afford the desired product.
49% With chloranil; In toluene; at 100℃; for 48h;Inert atmosphere; General procedure: IC-7-4 (20 g, 81.84 mmol) obtained in Step 1 and chloranil (72.25 g, 327.36 mmol) and toluene (400 ml) was stirred in a nitrogen stream for 2 days at 100 C . After the end of reaction vacuum filter to remove the chloranil method, removing the solvent from the filtrate was filtered by column chromatography (Hexane: MC = 5: 1 (v / v)) to give IC-7-3 (14.95 g, yield: 76 %). Instead of IC-7-4 (20 g, 81.84 mmol) the use of IC-12-4 (10 g, 39.62 mmol) the performs the same procedure as Step 2 Preparation Example 7 to obtain a IC-12-3 (9.68 g, yield 49%).
 

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