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N-(3-(2-(hydroxymethyl)phenyl)but-3-enyl)-4-methylbenzenesulfonamide

Base Information Edit
  • Chemical Name:N-(3-(2-(hydroxymethyl)phenyl)but-3-enyl)-4-methylbenzenesulfonamide
  • CAS No.:1628058-62-7
  • Molecular Formula:C18H21NO3S
  • Molecular Weight:331.436
  • Hs Code.:
  • Mol file:1628058-62-7.mol
N-(3-(2-(hydroxymethyl)phenyl)but-3-enyl)-4-methylbenzenesulfonamide

Synonyms:N-(3-(2-(hydroxymethyl)phenyl)but-3-enyl)-4-methylbenzenesulfonamide

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Chemical Property of N-(3-(2-(hydroxymethyl)phenyl)but-3-enyl)-4-methylbenzenesulfonamide Edit
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Technology Process of N-(3-(2-(hydroxymethyl)phenyl)but-3-enyl)-4-methylbenzenesulfonamide

There total 14 articles about N-(3-(2-(hydroxymethyl)phenyl)but-3-enyl)-4-methylbenzenesulfonamide 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 9 steps
1.1: 1H-imidazole / dichloromethane / 1.17 h / 0 - 20 °C
2.1: oxalyl dichloride; dimethyl sulfoxide / dichloromethane / 3 h / -78 - 20 °C
2.2: 2 h / 25 °C
3.1: lithium hexamethyldisilazane / tetrahydrofuran / 0.75 h / 0 °C
3.2: 23 °C
4.1: camphor-10-sulfonic acid / methanol / 0 °C
5.1: triethylamine; dmap / dichloromethane / 1 h / 0 - 20 °C
6.1: sodium azide / N,N-dimethyl-formamide / 8 h / 80 °C
7.1: triphenylphosphine / tetrahydrofuran; water / 12 h / 20 °C
8.1: triethylamine; dmap / dichloromethane / 3 h / 0 - 20 °C
9.1: pyridine; hydrogen fluoride / tetrahydrofuran / 12 h / 20 °C
With pyridine; 1H-imidazole; dmap; sodium azide; oxalyl dichloride; camphor-10-sulfonic acid; hydrogen fluoride; dimethyl sulfoxide; triethylamine; triphenylphosphine; lithium hexamethyldisilazane; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide; 2.1: |Swern Oxidation / 2.2: |Swern Oxidation;
DOI:10.1002/ejoc.201402157
Guidance literature:
Multi-step reaction with 7 steps
1.1: lithium hexamethyldisilazane / tetrahydrofuran / 0.75 h / 0 °C
1.2: 23 °C
2.1: camphor-10-sulfonic acid / methanol / 0 °C
3.1: triethylamine; dmap / dichloromethane / 1 h / 0 - 20 °C
4.1: sodium azide / N,N-dimethyl-formamide / 8 h / 80 °C
5.1: triphenylphosphine / tetrahydrofuran; water / 12 h / 20 °C
6.1: triethylamine; dmap / dichloromethane / 3 h / 0 - 20 °C
7.1: pyridine; hydrogen fluoride / tetrahydrofuran / 12 h / 20 °C
With pyridine; dmap; sodium azide; camphor-10-sulfonic acid; hydrogen fluoride; triethylamine; triphenylphosphine; lithium hexamethyldisilazane; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1002/ejoc.201402157
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