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Chemical Structure| 31931-53-0 Chemical Structure| 31931-53-0

Structure of 31931-53-0

Chemical Structure| 31931-53-0

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Product Details of [ 31931-53-0 ]

CAS No. :31931-53-0
Formula : C10H13NO2
M.W : 179.22
SMILES Code : O=C(C1C=C(C)C=NC=1C)OCC
MDL No. :MFCD16250719

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Application In Synthesis of [ 31931-53-0 ]

* 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 [ 31931-53-0 ]

[ 31931-53-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 31931-53-0 ]
  • [ 124796-97-0 ]
YieldReaction ConditionsOperation in experiment
63% With trichloroisocyanuric acid; In dichloromethane; at 20℃; for 16h; A mixture of ethyl 2,5-dimethylnicotinate (6.0 g, 33.52 mmol), 1,3,5-trichloro-1,3,5- triazinane-2,4,6-trione (11.3 g, 50.3 mmol) in DCM (200 mL) was stirred for 16 hr at RT. The mixture was poured into aqueous NaHCO3 solution (100 mL), the organic layer was dried over Na2504, concentrated and purified by column chromatograph on silica gel using 20% EA in PEas an eluent to afford ethyl 2-(chloromethyl)-5-methylnicotinate (4.5 g, 63.0%) as yellow oil. MS (ESI, m/e) [M+1] 214.0.
With trichloroisocyanuric acid; In dichloromethane; at 20 - 25℃; for 18h; As shown in step 11 -ii of Scheme 11 , Compound 2035 (354 mg, 1.98 mmol) and l,3,5-trichloro-l,3,5-triazinane-2,4,6-trione (689 mg, 2.96 mmol) were combined in DCM (1.8 mL). After stirring 18 hours at room temperature, the mixture was diluted with 20 mLs each of saturated sodium carbonate and dichloromethane. The organics were separated, washed with saturated sodium carbonate, washed with brine, dried over sodium sulfate, filtered, and concentrated under reduced pressure to give ethyl 2-(chloromethyl)-5- methylnicotinate (Compound 2036, 465 mg) as a pale yellow oil: ESMS (M+l) 213.86.
  • 2
  • [ 1721-26-2 ]
  • [ 20859-02-3 ]
  • [ 31931-53-0 ]
  • [ 545394-60-3 ]
 

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