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Chemical Structure| 126496-79-5 Chemical Structure| 126496-79-5

Structure of 126496-79-5

Chemical Structure| 126496-79-5

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Product Details of [ 126496-79-5 ]

CAS No. :126496-79-5
Formula : C9H15NO4
M.W : 201.22
SMILES Code : O=C(N1[C@H](C(OC)=O)C1)OC(C)(C)C
MDL No. :MFCD10566310
InChI Key :OHKDZMSOHBQKDL-UOQJWNSWSA-N
Pubchem ID :11701222

Safety of [ 126496-79-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 126496-79-5 ]

* 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 [ 126496-79-5 ]

[ 126496-79-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 6216-63-3 ]
  • [ 126496-79-5 ]
  • C22H32N2O7 [ No CAS ]
YieldReaction ConditionsOperation in experiment
56% In dichloromethane; for 16h; The (S)-2-(hydroxy methyl) pyrrolidine -1 - carboxylic acid benzyl ester 5 b (0.88 g, 3 . 73 mmol, using known method "Synthesis, 2013, 45 (17), 2458 - 2468" prepared) is dissolved in 10 ml dichloromethane in, cooling to 0 °C, adding boron trifluoride diethyl ether solution (63 mul, 498 mumol), stirring for 10 minutes, by adding 10 ml (S)-1 - tert-butyl 2 - methyl ethylene imine - 1, 2 - dicarboxylic ester 5 a (0.5 g, 2 . 49 mmol, using known method prepared by the) of the dichloromethane solution, 0 °C stirring reaction for 1 hour, raising the temperature to room temperature, stirring reaction for 16 hours. The reaction solution is added in 20 ml 1 M sodium hydroxide solution, stirring 15 minutes, layered, separating the organic phase, the aqueous phase is extracted with ethyl acetate, the combined organic phase, anhydrous sulfuric acid drying, filtering, the filtrate is concentrated under reduced pressure, to the silica gel column chromatography eluting system A purifying the obtained residue, to obtain the title product 5 c (0.61 g, yield: 56percent).
 

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