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toluene-4-sulfonic acid 2-[[3-(3-chloro-phenyl)-2-hydroxy-3-(2-methoxy-phenoxy)-propyl]-(toluene-4-sulfonyl)-amino]-ethyl ester

Base Information
  • Chemical Name:toluene-4-sulfonic acid 2-[[3-(3-chloro-phenyl)-2-hydroxy-3-(2-methoxy-phenoxy)-propyl]-(toluene-4-sulfonyl)-amino]-ethyl ester
  • CAS No.:863969-85-1
  • Molecular Formula:C32H34ClNO8S2
  • Molecular Weight:660.209
  • Hs Code.:
toluene-4-sulfonic acid 2-[[3-(3-chloro-phenyl)-2-hydroxy-3-(2-methoxy-phenoxy)-propyl]-(toluene-4-sulfonyl)-amino]-ethyl ester

Synonyms:

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Chemical Property of toluene-4-sulfonic acid 2-[[3-(3-chloro-phenyl)-2-hydroxy-3-(2-methoxy-phenoxy)-propyl]-(toluene-4-sulfonyl)-amino]-ethyl ester
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Technology Process of toluene-4-sulfonic acid 2-[[3-(3-chloro-phenyl)-2-hydroxy-3-(2-methoxy-phenoxy)-propyl]-(toluene-4-sulfonyl)-amino]-ethyl ester

There total 9 articles about toluene-4-sulfonic acid 2-[[3-(3-chloro-phenyl)-2-hydroxy-3-(2-methoxy-phenoxy)-propyl]-(toluene-4-sulfonyl)-amino]-ethyl ester 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 7 steps
1.1: aq. NaOH; methyltributylammonium chloride / CH2Cl2 / 2 h / 20 °C
1.2: 39 percent / 3 h / 65 °C
2.1: Et3N / ethyl acetate / 0.25 h / -20 °C
3.1: Et3N / ethyl acetate / 0.25 h / -20 °C
4.1: aq. HCl / ethyl acetate / -20 - 20 °C
5.1: aq. NaOH; methyltributylammonium chloride / toluene / 20 °C
6.1: 48 percent / propan-2-ol / Heating
7.1: Et3N / CH2Cl2
With hydrogenchloride; sodium hydroxide; triethylamine; methyl tributylammonium chloride; In dichloromethane; ethyl acetate; isopropyl alcohol; toluene;
DOI:10.1016/j.tetasy.2005.06.012
Guidance literature:
Multi-step reaction with 2 steps
1: 48 percent / propan-2-ol / Heating
2: Et3N / CH2Cl2
With triethylamine; In dichloromethane; isopropyl alcohol;
DOI:10.1016/j.tetasy.2005.06.012
Guidance literature:
Multi-step reaction with 6 steps
1: Et3N / ethyl acetate / 0.25 h / -20 °C
2: Et3N / ethyl acetate / 0.25 h / -20 °C
3: aq. HCl / ethyl acetate / -20 - 20 °C
4: aq. NaOH; methyltributylammonium chloride / toluene / 20 °C
5: 48 percent / propan-2-ol / Heating
6: Et3N / CH2Cl2
With hydrogenchloride; sodium hydroxide; triethylamine; methyl tributylammonium chloride; In dichloromethane; ethyl acetate; isopropyl alcohol; toluene;
DOI:10.1016/j.tetasy.2005.06.012
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