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tert-butyl syn-2-hydroxy-3-phenyl-3-(tosylamino)propanoate

Base Information Edit
  • Chemical Name:tert-butyl syn-2-hydroxy-3-phenyl-3-(tosylamino)propanoate
  • CAS No.:203176-12-9
  • Molecular Formula:C20H25NO5S
  • Molecular Weight:391.488
  • Hs Code.:
  • Mol file:203176-12-9.mol
tert-butyl syn-2-hydroxy-3-phenyl-3-(tosylamino)propanoate

Synonyms:tert-butyl syn-2-hydroxy-3-phenyl-3-(tosylamino)propanoate

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Chemical Property of tert-butyl syn-2-hydroxy-3-phenyl-3-(tosylamino)propanoate Edit
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Technology Process of tert-butyl syn-2-hydroxy-3-phenyl-3-(tosylamino)propanoate

There total 3 articles about tert-butyl syn-2-hydroxy-3-phenyl-3-(tosylamino)propanoate 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:
rac-2,3-bis(tosylamino)-succinic acid; With potassium carbonate; K2; In water; tert-butyl alcohol; at 20 ℃; for 0.25h;
tert-butyl cinnamate; With chloroamine-T; In water; tert-butyl alcohol; at 20 ℃; for 20h; Title compound not separated from byproducts;
DOI:10.1002/adsc.200606054
Guidance literature:
(S)-N,N'-bistosyl-2,3-diaminopropionic acid; With potassium carbonate; K2; In water; tert-butyl alcohol; at 20 ℃; for 0.25h;
tert-butyl cinnamate; With chloroamine-T; In water; tert-butyl alcohol; at 20 ℃; for 20h; Title compound not separated from byproducts;
DOI:10.1002/adsc.200606054
Guidance literature:
Multi-step reaction with 2 steps
1.1: 57 percent / aq. LiOH / 40 h / 20 °C
2.1: K2CO3 / K2[OsO2(OH)4] / H2O; 2-methyl-propan-2-ol / 0.25 h / 20 °C
2.2: chloramine T / H2O; 2-methyl-propan-2-ol / 20 h / 20 °C
With lithium hydroxide; potassium carbonate; K2; In water; tert-butyl alcohol;
DOI:10.1002/adsc.200606054
upstream raw materials:

tert-butyl cinnamate

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