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3-[3-[5-benzyloxy-2-ethyl-4-(4-fluorophenyl)phenoxy]propoxy]-2-propylbenzamide

Base Information
  • Chemical Name:3-[3-[5-benzyloxy-2-ethyl-4-(4-fluorophenyl)phenoxy]propoxy]-2-propylbenzamide
  • CAS No.:1447666-98-9
  • Molecular Formula:C34H36FNO4
  • Molecular Weight:541.663
  • Hs Code.:
3-[3-[5-benzyloxy-2-ethyl-4-(4-fluorophenyl)phenoxy]propoxy]-2-propylbenzamide

Synonyms:3-[3-[5-benzyloxy-2-ethyl-4-(4-fluorophenyl)phenoxy]propoxy]-2-propylbenzamide

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Chemical Property of 3-[3-[5-benzyloxy-2-ethyl-4-(4-fluorophenyl)phenoxy]propoxy]-2-propylbenzamide
Chemical Property:
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Technology Process of 3-[3-[5-benzyloxy-2-ethyl-4-(4-fluorophenyl)phenoxy]propoxy]-2-propylbenzamide

There total 8 articles about 3-[3-[5-benzyloxy-2-ethyl-4-(4-fluorophenyl)phenoxy]propoxy]-2-propylbenzamide 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:
3-[3-[5-benzyloxy-2-ethyl-4-(4-fluorophenyl)phenoxy]propoxy]-2-propylbenzoic acid; With thionyl chloride; N,N-dimethyl-formamide; In tetrahydrofuran; at 0 - 5 ℃; for 1h;
With ammonium hydroxide; In tetrahydrofuran; methanol; water; at 0 - 5 ℃; for 0.5h;
Guidance literature:
Multi-step reaction with 6 steps
1.1: acetic acid / tetrahydrofuran; diethyl ether / 3.5 h / -12 - -10 °C
2.1: boron tribromide / toluene / 3 h / -25 - -5 °C
2.2: 0.5 h / 7 °C
3.1: thionyl chloride / 35.5 h / -10 °C
4.1: potassium carbonate; dmap / dimethyl sulfoxide / 87 h / 60 °C
5.1: potassium hydroxide / 1-methyl-pyrrolidin-2-one / 0.42 h / 120 °C
6.1: N,N-dimethyl-formamide; thionyl chloride / tetrahydrofuran / 1 h / 0 - 5 °C
6.2: 0.5 h / 0 - 5 °C
With dmap; thionyl chloride; boron tribromide; potassium carbonate; acetic acid; N,N-dimethyl-formamide; potassium hydroxide; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; diethyl ether; dimethyl sulfoxide; toluene;
Guidance literature:
Multi-step reaction with 8 steps
1.1: N,N-dimethyl-formamide; thionyl chloride / toluene / 1 h / 40 °C
2.1: pyridine; dmap / dichloromethane / 1.08 h / Reflux
3.1: acetic acid / tetrahydrofuran; diethyl ether / 3.5 h / -12 - -10 °C
4.1: boron tribromide / toluene / 3 h / -25 - -5 °C
4.2: 0.5 h / 7 °C
5.1: thionyl chloride / 35.5 h / -10 °C
6.1: potassium carbonate; dmap / dimethyl sulfoxide / 87 h / 60 °C
7.1: potassium hydroxide / 1-methyl-pyrrolidin-2-one / 0.42 h / 120 °C
8.1: N,N-dimethyl-formamide; thionyl chloride / tetrahydrofuran / 1 h / 0 - 5 °C
8.2: 0.5 h / 0 - 5 °C
With pyridine; dmap; thionyl chloride; boron tribromide; potassium carbonate; acetic acid; N,N-dimethyl-formamide; potassium hydroxide; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; diethyl ether; dichloromethane; dimethyl sulfoxide; toluene;
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