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Chemical Structure| 128510-88-3 Chemical Structure| 128510-88-3

Structure of 128510-88-3

Chemical Structure| 128510-88-3

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Product Details of [ 128510-88-3 ]

CAS No. :128510-88-3
Formula : C17H25NO5S
M.W : 355.45
SMILES Code : O=C(N1[C@@H](COS(=O)(C2=CC=C(C)C=C2)=O)CCC1)OC(C)(C)C
MDL No. :MFCD11505914

Safety of [ 128510-88-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H332-H335
Precautionary Statements:P261-P280-P305+P351+P338

Application In Synthesis of [ 128510-88-3 ]

* 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 [ 128510-88-3 ]

[ 128510-88-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 128510-88-3 ]
  • [ 137496-71-0 ]
YieldReaction ConditionsOperation in experiment
79% With lithium triethylborohydride; In tetrahydrofuran; at 0℃; for 15.0h; Step 3: Preparation of 2-(S)-methyl-pyrrolidine-1-carboxylic Tert-butyl Ester (5) To a solution of 2-(S)-(toluene-4-sulfonyloxymethyl)-pyrrolidine-1-carboxylic acid tert-butyl ester (compound (4), 1.77 g, 4.99 mmol) in 5 ML of THF at 0 C. was added dropwise 15 ML (15 mmol) of a 1 M THF solution of lithium triethylborohydride.After 15 hours, the reaction was quenched by addition of 7.39 ML of water.The reaction was diluted with 35 ML of chloroform, and poured into a separatory funnel.The mixture was diluted with dichloromethane and washed with saturated aqueous NaCl solution.The organic phase then was dried over sodium sulfate.The mixture was concentrated in vacuo and purified by flash chromatography on silica gel, eluding with 1:3 ethyl acetate/hexane to give pure product as a clear oil (0.73 g, 79% yield).
79% With lithium triethylborohydride; In tetrahydrofuran; at 0℃; for 15.0h; Step 3: Preparation of 2-(S)-methyl-pyrrolidine-1-carboxylic tert-butyl ester (5) To a solution of 2-(S)-(toluene-4-sulfonyloxymethyl)-pyrrolidine- 1-carboxylic acid tert-butyl ester (compound (4), 1.77 g, 4.99 mmol) in 5 mL of THF at 0 C. was added dropwise 15 mL (15 mmol) of a 1 M THF solution of lithium triethylborohydride. After 15 hours, the reaction was quenched by addition of 7.39 mL of water. The reaction was diluted with 35 mL of chloroform, and poured into a separatory funnel. The mixture was diluted with dichloromethane and washed with saturated aqueous NaCl solution. The organic phase then was dried over sodium sulfate. The mixture was concentrated in vacuo and purified by flash chromatography on silica gel, eluding with 1:3 ethyl acetate/hexane to give pure product as a clear oil (0.73 g, 79% yield).
 

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