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Chemical Structure| 1007388-28-4 Chemical Structure| 1007388-28-4

Structure of 1007388-28-4

Chemical Structure| 1007388-28-4

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Product Details of [ 1007388-28-4 ]

CAS No. :1007388-28-4
Formula : C5H5FOS
M.W : 132.16
SMILES Code : OCC1=CC(F)=CS1
MDL No. :MFCD26386077

Safety of [ 1007388-28-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 1007388-28-4 ]

* 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 [ 1007388-28-4 ]

[ 1007388-28-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 32431-75-7 ]
  • [ 1007388-28-4 ]
YieldReaction ConditionsOperation in experiment
77.6% With sodium tetrahydroborate; ethanol; at 0 - 20℃; for 16.5h; Into a 1000-mL round-bottom flask, was placed <strong>[32431-75-7]methyl 4-fluorothiophene-2-carboxylate</strong> (10 g, 62.4 mmol) in ethanol (300 mL). Then to the above solution was added NaBH4(4.62 g, 125 mmol) in portions at 0C in an ice/ethanol bath. The resulting solution was stirred for 30 min at 0C and then the reaction solution was allowed to react for an additional 16 h at RT. The reaction was then quenched by the addition of 50 mL of water. Then the mixture was concentrated and extracted with 3xl00mL of ethyl acetate and the organic layers were combined and dried over anhydrous sodium sulfate and concentrated under vacuum. This resulted in 6.4 g (77.6%) of the title compound as white oil. MS-ESI: 133 (M+l)
77.5% With sodium tetrahydroborate; ethanol; at 0 - 20℃; for 16.5h;Inert atmosphere; Into a 1000-mL 3-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed <strong>[32431-75-7]methyl 4-fluorothiophene-2-carboxylate</strong> (10 g, 62.4 mmol) in EtOH (300 mL). To the above solution was added NaBH4 (4.74 g, 124.8 mmol) with stirring at 0C. Theresulting solution was stirred for 30 mm at 0C. The resulting solution was allowed to react for an additional 16 h at RT. The reaction was then quenched by the addition of 10 mL of water. The resulting mixture was extracted with 3x1000 mL of ethyl acetate. Evaporation of combined ethyl acetate solution resulted in 6.4 g (77.5%) of the title compound as white oil.
 

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