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Chemical Structure| 143656-79-5 Chemical Structure| 143656-79-5

Structure of 143656-79-5

Chemical Structure| 143656-79-5

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Product Details of [ 143656-79-5 ]

CAS No. :143656-79-5
Formula : C12H16N2O3
M.W : 236.27
SMILES Code : O=C(N1CC(N)C(O)C1)OCC2=CC=CC=C2

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Application In Synthesis of [ 143656-79-5 ]

* 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 [ 143656-79-5 ]

[ 143656-79-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 31865-25-5 ]
  • [ 143656-79-5 ]
YieldReaction ConditionsOperation in experiment
85.92% With ammonium hydroxide; at 100℃; for 16h; Benzyl 6-oxa-3-azabicyclo[3.1.0]hexane-3-carboxylate (5.40 g, 24.63 mmol, 1.00 eq) and ammonia (43.17 g, 1.23 mol, 47.43 mL, 50.00 eq) were mixed, the mixture was then stirred at 100 C for 16 hours. The mixture was concentrated under reduced pressure to deliver benzyl 3-amino-4-hydroxy-pyrrolidine-1-carboxylate (5.00 g, 21.16 mmol, 85.92% yield) as a slightly yellow oil.
With ammonia; In water; for 4h;Reflux; A mixture of benzyl 6-oxa-3-aza-bicyclo[3.1.0]hexane-3-carboxylate (5 g, 23 mmol) and aqueous ammonia (60 mL) was heated at reflux for 4 h. The solution was concentrated in vacuo to afford the crude product benzyl 3-amino-4-hydroxypyrrolidine- 1-carboxylate as a light oil, which was used without further purification (5 g, 93%).
6.1 g With ammonium hydroxide; for 20h;Sealed tube; 6.01.28.04 Benzyl 3-amino-4-hydroxypyrrolidine-1-carboxylate 6.5 g <strong>[31865-25-5]benzyl 6-oxa-3-azabicyclo[3.1.0]hexane-3-carboxylate</strong> in 80 mL 33% aqueous ammonia solution was stirred 20 h in a closed vessel. The reaction was cooled and extracted with dichlormethane. The organic layer was washed with sodium chloride solution and evaporated to give 6.1 g of the desired product. Rt: 2.37 min. (method AG)
 

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