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Chemical Structure| 102625-99-0 Chemical Structure| 102625-99-0

Structure of 102625-99-0

Chemical Structure| 102625-99-0

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Product Details of [ 102625-99-0 ]

CAS No. :102625-99-0
Formula : C10H13NO4
M.W : 211.22
SMILES Code : CC(OCC1=NC=CC(OC)=C1OC)=O
MDL No. :MFCD25954419

Safety of [ 102625-99-0 ]

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

Application In Synthesis of [ 102625-99-0 ]

* 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 [ 102625-99-0 ]

[ 102625-99-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 102625-99-0 ]
  • [ 72830-08-1 ]
YieldReaction ConditionsOperation in experiment
With sodium hydroxide; In Petroleum ether; (b) 2-Hydroxymethyl-3,4-dimethoxypyridine After adding 15 ml of 2N sodium hydroxide solution, 4.8 g of 2-acetoxymethyl-3,4-dimethoxypyridine are stirred vigorously at 80 C., whereupon a homogeneous solution forms from the initial two-phase mixture. After 2 hours, the solution is allowed to cool and is extracted five times with 30 ml of methylene chloride each time, the combined organic phases are washed twice with 5 ml of 0.3N sodium hydroxide solution each time, dried over potassium carbonate, filtered and concentrated and the distillation residue is stirred with petroleum ether. 3.6 g (96% of theory) of 2-hydroxymethyl-3,4-dimethoxypyridine are obtained as a colourless solid of m.p. 87-89 C.
With sodium hydroxide; In Petroleum ether; (b) 2-Hydroxymethyl-3,4-dimethoxypyridine After adding 15 ml of 2N sodium hydroxide solution, 4.8 g of 2-acetoxymethyl-3,4-dimethoxypyridine are stirred vigorously at 80 C., whereupon a homogeneous solution forms from the initial two-phase mixture. After 2 hours, the solution is allowed to cool and is extracted five times with 30 ml of methylene chloride each time, the combined organic phases are washed twice with 5 ml of 0.3N sodium hydroxide solution each time, dried over potassium carbonate, filtered and concentrated and the distillation residue is stirred with petroleum ether. 3.6 g (96% of theory) of 2-hydroxymethyl-3,4-dimethoxy-pyridine are obtained as a colorless solid of m.p. 87-89 C.
 

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