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Chemical Structure| 960401-34-7 Chemical Structure| 960401-34-7

Structure of 960401-34-7

Chemical Structure| 960401-34-7

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Product Details of [ 960401-34-7 ]

CAS No. :960401-34-7
Formula : C15H20N2O6
M.W : 324.33
SMILES Code : O=[N+](C1=CC=C(OC2CN(C(OC(C)(C)C)=O)C2)C(OC)=C1)[O-]
MDL No. :MFCD12965041

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Application In Synthesis of [ 960401-34-7 ]

* 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 [ 960401-34-7 ]

[ 960401-34-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 454-16-0 ]
  • [ 141699-55-0 ]
  • [ 960401-34-7 ]
YieldReaction ConditionsOperation in experiment
95% With potassium tert-butylate; In tetrahydrofuran; at 0℃; for 0.5h; Dissolve l-fluoro-2-methoxy-4-nitro-benzene (118 g, 689 mmol) and 3-hydroxy- azetidine-1-carboxylic acid tert-bupsilonXyl ester (125 g, 724 mmol) in THF (800 mL) and cool to 0 0C under nitrogen. To the above solution, add dropwise a 1 M THF solution of tert- BuOK (1 L). After the addition is complete, stir the dark brown solution for 30 min at 0 0C and then dilute with water (1 L) over a 10 min period. Stir the mixture for 5 min, then extract with tert-bvAyl methyl ether (2x ). Combine the organic solutions and wash with brine (2 x 700 mL), then dry and concentrate. Dry the solid in vacuo at 45 0C for 20 h to obtain 216 g (95percent) of the title compound as a yellow solid. 1H NMR (300 MHz, CDCl3) 6.47 (d, IH, J= 8.5), 6.30 (d, IH, J= 2.6), 6.17 (dd, IH, J= 2.4, 8.5), 4.76 (m, IH), 4.18 (m, 2H), 4.04 (m, 2H), 3.80 (s, 3H), 1.42 (s, 9H).
95% With potassium tert-butylate; In tetrahydrofuran; at 0℃; for 0.5h; Preparation 60; 3-(2-Methoxy-4-nitro-phenoxy)-azetidine-l-carboxylic acid tert-butyl ester; Dissolve l-fluoro-2-methoxy-4-nitro-benzene (118 g, 689 mmol) and 3 -hydroxy - azetidine-1-carboxylic acid tert-butyl ester (125 g, 724 mmol) in THF (800 mL) and cool to 0 0C. To the above solution under a nitrogen atmosphere, add dropwise a IM solution of tBuOK (I L, solution in THF). After addition is complete, stir the dark brown solution for 30 min at 0 0C, then dilute with water (1 L) over a 10 min period. Stir the mixture for5 min, then extract with MTBE twice. Combine the organic solutions and wash with brine (2 x 700 mL), then dry and concentrate. Dry the solid in vacuo at 45 0C for 20 h to <n="56"/>obtain 216 g (95percent) of the title compounds as a yellow solid. 1H NMR (300 MHz, CDCl3) .pound. 1.42 (s, 9H), 3.80 (s, 3H), 4.04 (m, 2H), 4.18 (m, 2H), 4.76 (m, IH), 6.17 (dd, IH, J = 2.4, 8.5), 6.30 (d, IH, J= 2.6), 6.47 (d, IH, J= 8.5).
 

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