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5-benzyl 2-tert-butyl (4R)-1-oxo-2,5-diazaspiro[3.4]octane-2,5-dicarboxylate

Base Information Edit
  • Chemical Name:5-benzyl 2-tert-butyl (4R)-1-oxo-2,5-diazaspiro[3.4]octane-2,5-dicarboxylate
  • CAS No.:914389-51-8
  • Molecular Formula:C19H24N2O5
  • Molecular Weight:360.41
  • Hs Code.:
  • Mol file:914389-51-8.mol
5-benzyl 2-tert-butyl (4R)-1-oxo-2,5-diazaspiro[3.4]octane-2,5-dicarboxylate

Synonyms:(4R)-5-benzyloxycarbonyl-2-(tert-butoxycarbonyl)-2,5-diazaspiro[3,4]octan-1-one

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Chemical Property of 5-benzyl 2-tert-butyl (4R)-1-oxo-2,5-diazaspiro[3.4]octane-2,5-dicarboxylate Edit
Chemical Property:
  • Vapor Pressure:1.95E-11mmHg at 25°C 
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Technology Process of 5-benzyl 2-tert-butyl (4R)-1-oxo-2,5-diazaspiro[3.4]octane-2,5-dicarboxylate

There total 6 articles about 5-benzyl 2-tert-butyl (4R)-1-oxo-2,5-diazaspiro[3.4]octane-2,5-dicarboxylate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Multi-step reaction with 6 steps
1.1: BF3*Et2O / CH2Cl2 / 12 h / -40 - 20 °C
2.1: 98 percent / H2 / Pd/C / ethyl acetate; methanol / 760 Torr
3.1: L-Boc-Phe-OH / ethyl acetate; hexane
3.2: aq. NaHCO3 / CH2Cl2 / 0.17 h
4.1: 97 percent / NaHCO3 / ethyl acetate; H2O / 2 h / 20 °C
5.1: aq. CAN / acetonitrile / 0 °C
6.1: 0.652 g / DMAP / acetonitrile / 0 - 20 °C
With dmap; ammonium cerium(IV) nitrate; N-tert-butoxycarbonyl-L-phenylalanine; boron trifluoride diethyl etherate; hydrogen; sodium hydrogencarbonate; palladium on activated charcoal; In methanol; hexane; dichloromethane; water; ethyl acetate; acetonitrile;
DOI:10.1021/jo061189l
Guidance literature:
Multi-step reaction with 5 steps
1.1: 98 percent / H2 / Pd/C / ethyl acetate; methanol / 760 Torr
2.1: L-Boc-Phe-OH / ethyl acetate; hexane
2.2: aq. NaHCO3 / CH2Cl2 / 0.17 h
3.1: 97 percent / NaHCO3 / ethyl acetate; H2O / 2 h / 20 °C
4.1: aq. CAN / acetonitrile / 0 °C
5.1: 0.652 g / DMAP / acetonitrile / 0 - 20 °C
With dmap; ammonium cerium(IV) nitrate; N-tert-butoxycarbonyl-L-phenylalanine; hydrogen; sodium hydrogencarbonate; palladium on activated charcoal; In methanol; hexane; water; ethyl acetate; acetonitrile;
DOI:10.1021/jo061189l
Guidance literature:
Multi-step reaction with 7 steps
1.1: Et3N / CH2Cl2 / 0.75 h / -40 °C
2.1: BF3*Et2O / CH2Cl2 / 12 h / -40 - 20 °C
3.1: 98 percent / H2 / Pd/C / ethyl acetate; methanol / 760 Torr
4.1: L-Boc-Phe-OH / ethyl acetate; hexane
4.2: aq. NaHCO3 / CH2Cl2 / 0.17 h
5.1: 97 percent / NaHCO3 / ethyl acetate; H2O / 2 h / 20 °C
6.1: aq. CAN / acetonitrile / 0 °C
7.1: 0.652 g / DMAP / acetonitrile / 0 - 20 °C
With dmap; ammonium cerium(IV) nitrate; N-tert-butoxycarbonyl-L-phenylalanine; boron trifluoride diethyl etherate; hydrogen; sodium hydrogencarbonate; triethylamine; palladium on activated charcoal; In methanol; hexane; dichloromethane; water; ethyl acetate; acetonitrile;
DOI:10.1021/jo061189l
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