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3-t-butyl-4-methoxy-5-methylsulfonylbenzoyl chloride

Base Information
  • Chemical Name:3-t-butyl-4-methoxy-5-methylsulfonylbenzoyl chloride
  • CAS No.:1285575-37-2
  • Molecular Formula:C13H17ClO4S
  • Molecular Weight:304.795
  • Hs Code.:
3-t-butyl-4-methoxy-5-methylsulfonylbenzoyl chloride

Synonyms:3-t-butyl-4-methoxy-5-methylsulfonylbenzoyl chloride

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Chemical Property of 3-t-butyl-4-methoxy-5-methylsulfonylbenzoyl chloride
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Technology Process of 3-t-butyl-4-methoxy-5-methylsulfonylbenzoyl chloride

There total 7 articles about 3-t-butyl-4-methoxy-5-methylsulfonylbenzoyl chloride 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:
With thionyl chloride; N,N-dimethyl-formamide; In toluene; at 60 ℃; for 16h;
Guidance literature:
Multi-step reaction with 7 steps
1.1: methanesulfonic acid / 16 h / 70 °C
1.2: 3 h / 50 °C
2.1: N-iodo-succinimide; trifluorormethanesulfonic acid / methanol; dichloromethane / 0.25 h / 20 °C
3.1: zinc / [2,2]bipyridinyl; nickel dibromide / N,N-dimethyl-formamide / 1 h / 130 °C
4.1: potassium carbonate / N,N-dimethyl-formamide / 20 h / 20 °C
5.1: 3-chloro-benzenecarboperoxoic acid / chloroform / 3 h / 20 °C
6.1: lithium hydroxide monohydrate; water / tetrahydrofuran / 5 h / 20 °C
7.1: thionyl chloride / N,N-dimethyl-formamide / toluene / 16 h / 60 °C
With N-iodo-succinimide; thionyl chloride; methanesulfonic acid; lithium hydroxide monohydrate; trifluorormethanesulfonic acid; water; potassium carbonate; 3-chloro-benzenecarboperoxoic acid; zinc; [2,2]bipyridinyl; N,N-dimethyl-formamide; nickel dibromide; In tetrahydrofuran; methanol; dichloromethane; chloroform; N,N-dimethyl-formamide; toluene;
Guidance literature:
Multi-step reaction with 6 steps
1: N-iodo-succinimide; trifluorormethanesulfonic acid / methanol; dichloromethane / 0.25 h / 20 °C
2: zinc / [2,2]bipyridinyl; nickel dibromide / N,N-dimethyl-formamide / 1 h / 130 °C
3: potassium carbonate / N,N-dimethyl-formamide / 20 h / 20 °C
4: 3-chloro-benzenecarboperoxoic acid / chloroform / 3 h / 20 °C
5: lithium hydroxide monohydrate; water / tetrahydrofuran / 5 h / 20 °C
6: thionyl chloride / N,N-dimethyl-formamide / toluene / 16 h / 60 °C
With N-iodo-succinimide; thionyl chloride; lithium hydroxide monohydrate; trifluorormethanesulfonic acid; water; potassium carbonate; 3-chloro-benzenecarboperoxoic acid; zinc; [2,2]bipyridinyl; N,N-dimethyl-formamide; nickel dibromide; In tetrahydrofuran; methanol; dichloromethane; chloroform; N,N-dimethyl-formamide; toluene;
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