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propan-2-yl N-{2-[(tert-butoxycarbonyl)amino]-2-(3,5-difluorophenyl)propyl}-O-[tert-butyl(dimethyl)silyl]-2-methylserinate

Base Information
  • Chemical Name:propan-2-yl N-{2-[(tert-butoxycarbonyl)amino]-2-(3,5-difluorophenyl)propyl}-O-[tert-butyl(dimethyl)silyl]-2-methylserinate
  • CAS No.:1189569-93-4
  • Molecular Formula:C27H46F2N2O5Si
  • Molecular Weight:544.755
  • Hs Code.:
propan-2-yl N-{2-[(tert-butoxycarbonyl)amino]-2-(3,5-difluorophenyl)propyl}-O-[tert-butyl(dimethyl)silyl]-2-methylserinate

Synonyms:propan-2-yl N-{2-[(tert-butoxycarbonyl)amino]-2-(3,5-difluorophenyl)propyl}-O-[tert-butyl(dimethyl)silyl]-2-methylserinate

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Chemical Property of propan-2-yl N-{2-[(tert-butoxycarbonyl)amino]-2-(3,5-difluorophenyl)propyl}-O-[tert-butyl(dimethyl)silyl]-2-methylserinate
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Technology Process of propan-2-yl N-{2-[(tert-butoxycarbonyl)amino]-2-(3,5-difluorophenyl)propyl}-O-[tert-butyl(dimethyl)silyl]-2-methylserinate

There total 6 articles about propan-2-yl N-{2-[(tert-butoxycarbonyl)amino]-2-(3,5-difluorophenyl)propyl}-O-[tert-butyl(dimethyl)silyl]-2-methylserinate 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:
tert-butyl [1-(3,5-difluorophenyl)-1-methyl-2-oxoethyl]carbamate; methyl O-[(tert-butyl)(dimethyl)silyl]-2-methylserinate; titanium(IV) isopropylate; In ethyl acetate; at 20 ℃; for 2h;
With sodium cyanoborohydride; acetic acid; In methanol; at 0 - 20 ℃; for 0.533333h; Cooling;
Guidance literature:
Multi-step reaction with 4 steps
1.1: dichloromethane / 0 - 20 °C
1.2: 60 - 70 °C
2.1: potassium tert-butylate / tetrahydrofuran / -78 - 20 °C
2.2: -78 - 0 °C
3.1: lithium aluminium tetrahydride / tetrahydrofuran / 3 h / -78 °C
4.1: titanium(IV) isopropylate / ethyl acetate / 2 h / 20 °C
4.2: 0.53 h / 0 - 20 °C / Cooling
With lithium aluminium tetrahydride; potassium tert-butylate; titanium(IV) isopropylate; In tetrahydrofuran; dichloromethane; ethyl acetate;
Guidance literature:
Multi-step reaction with 4 steps
1.1: dichloromethane / 0 - 20 °C
1.2: 60 - 70 °C
2.1: potassium tert-butylate / tetrahydrofuran / -78 - 20 °C
2.2: -78 - 0 °C
3.1: lithium aluminium tetrahydride / tetrahydrofuran / 3 h / -78 °C
4.1: titanium(IV) isopropylate / ethyl acetate / 2 h / 20 °C
4.2: 0.53 h / 0 - 20 °C / Cooling
With lithium aluminium tetrahydride; potassium tert-butylate; titanium(IV) isopropylate; In tetrahydrofuran; dichloromethane; ethyl acetate;
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