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Chemical Structure| 1025351-41-0 Chemical Structure| 1025351-41-0

Structure of 1025351-41-0

Chemical Structure| 1025351-41-0

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Product Details of [ 1025351-41-0 ]

CAS No. :1025351-41-0
Formula : C5H5ClN2O
M.W : 144.56
SMILES Code : OCC1=NC=NC(Cl)=C1
MDL No. :MFCD20482236

Safety of [ 1025351-41-0 ]

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

Application In Synthesis of [ 1025351-41-0 ]

* 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 [ 1025351-41-0 ]

[ 1025351-41-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 6627-22-1 ]
  • [ 1025351-41-0 ]
YieldReaction ConditionsOperation in experiment
60% With sodium tetrahydroborate; ethanol; In tetrahydrofuran; at 0℃; for 3h; [0780] Into a 3000-mL 4-necked round-bottom flask was placed methyl 6-chloropyrimidine-4- carboxylate (80 g, 463.58 mmol, 1.00 equiv), tetrahydrofuran (1600 mL), and ethanol (160 mL) followed by the addition of NaBH4 (48 g, 1.27 mol, 3.00 equiv) in several batches at 0C. The resulting solution was stirred at 0C for 3 h, quenched by the addition of 1500 mL of water/ice, and extracted with 3x800 mL of ethyl acetate. The combined organic layers were washed with 1x800of brine, dried over anhydrous sodium sulfate, and concentrated under vacuum. The residue was applied onto a silica gel colunm eluted with ethyl acetate/petroleum ether (1:2) to afford 40 g (60%) of (6-chloropyrimidin-4-yl)methanol as a yellow solid. LCMS [M+H] 145.
60% With sodium tetrahydroborate; ethanol; In tetrahydrofuran; at 0℃; for 3h; Into a 3000-mL 4-necked round-bottom flask was placed methyl 6-chloropyrimidine-4- carboxylate (80 g, 463.58 mmol, 1.00 equiv), tetrahydrofuran (1600 mL), and ethanol (160 mL), followed by the addition of NaBH4 (48 g, 1.27 mol, 3.00 equiv) in several batches at 0C. The resulting solution was stirred at 0C for 3 h, quenched by the addition of 1500 mL of water/ice, and extracted with 3x800 mL of ethyl acetate. The combined organic layers were washed with 1x800 mL of brine, dried over anhydrous sodium sulfate, and concentrated under vacuum. The residue was applied onto a silica gel column eluted with ethyl acetate/petroleum ether (1 :2) to afford 40 g (60%) of (6-chloropyrimidin-4-yl)methanol as a yellow solid. LCMS [M+H]+ 145
 

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