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Chemical Structure| 186132-96-7 Chemical Structure| 186132-96-7

Structure of Boc-cis-3-OH-Pro-OH
CAS No.: 186132-96-7

Chemical Structure| 186132-96-7

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Product Details of [ 186132-96-7 ]

CAS No. :186132-96-7
Formula : C10H17NO5
M.W : 231.25
SMILES Code : CC(C)(C)OC(=O)N1CC[C@@H](O)[C@H]1C(O)=O
MDL No. :MFCD08458682
InChI Key :JLDHXHPQMBNKMC-RQJHMYQMSA-N
Pubchem ID :11096439

Safety of [ 186132-96-7 ]

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

Application In Synthesis of [ 186132-96-7 ]

* 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 [ 186132-96-7 ]

[ 186132-96-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 186132-96-7 ]
  • [ 567-35-1 ]
  • 2
  • [ 24424-99-5 ]
  • [ 567-35-1 ]
  • [ 186132-96-7 ]
YieldReaction ConditionsOperation in experiment
With triethylamine; In methanol; at 20℃; for 23.5h;Reflux; General procedure: To a stirred solution of trans-L-4-hydroxyproline i (2.0 g,15.3 mmol) in MeOH (36.0 mL) was added Et3N (4.0 mL,28.7 mmol) and Boc anhydride (6.7 g, 30.5 mmol) and the reaction was refluxed for 3.5 h, cooled to room temperature, and stirred for 20 h. Solvent was removed under vacuum and the residue cooled to 0oC. Following the addition of NaH2PO4 (150 mg), the solution was acidified to pH 2 with 0.5 M HCl.The mixture was stirred at 0oC for 30 min before extractingthe product with EtOAc (420 mL). The combined organic layers were dried with MgSO4 and filtered. The solvent was removed under vacuum yielding v as a white foam (3.23 g,14 mmol, 92 %)
 

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