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Chemical Structure| 136024-60-7 Chemical Structure| 136024-60-7

Structure of 136024-60-7

Chemical Structure| 136024-60-7

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Product Details of [ 136024-60-7 ]

CAS No. :136024-60-7
Formula : C18H25NO5
M.W : 335.39
SMILES Code : O=C(N1[C@H](C(OC)=O)C[C@@H](OCC2=CC=CC=C2)C1)OC(C)(C)C
MDL No. :MFCD11053516

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Application In Synthesis of [ 136024-60-7 ]

* 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 [ 136024-60-7 ]

[ 136024-60-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 136024-60-7 ]
  • [ 40350-83-2 ]
YieldReaction ConditionsOperation in experiment
97% With lithium hydroxide monohydrate; In tetrahydrofuran; at 20℃; for 3h; To a solution of compound 2 (3.45 g, 10.29 mmol) in THF: H2O (60 mL, 2:1) lithium hydroxide monohydrate (1.29 g, 30.87 mmol) was added and the reaction mixture was stirred at room temperature for 3 h. After completion of the reaction as indicated by TLC the reaction mixture was concentrated under reduced pressure, acidified with 1N hydrochloric acid and extracted with ethyl acetate. The organic layers were separated, washed with brine, dried over Na2SO4 and concentrated under reduced pressure to obtain the crude residue. The residue was purified by trituration with pentene to afford compound 3 (3.21 g, 97%). MS (ESI) m/z 322 [M+1]+.
76% b) (2S,4 ?)-4-(Benzyloxy)-1 -(ferf-butoxycarbonyl)pyrrolidine-2-carboxylic acid(2S,4 ?)-1 -ierf-Butyl 2-methyl 4-(benzyloxy)pyrrolidine-1 ,2-dicarboxylate (2.78 g, 8.29 mmol) was dissolved in a 1 :1 mixture of MeOH and THF (30 ml) and 2N NaOH (12.5 ml, 26 mmol) was added. After stirring at room temperature for 2h, the organic solvents were evaporated under reduced pressure and the aqueous phase was extracted twice with dichloromethane. The aqueous phase was then cooled at 0 C and then acidified with concentrated chlorhydric acid. This phase was extracted twice with dichloromethane. The organic phase was dried over magnesium sulphate, filtered and the solvent evaporated under reduced pressure. 2.01 g (76% yield) of the final compound were obtained, pure enough to perform the next synthetic step.LRMS (m/z): 322 (M+1 )+
 

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