N-[(3E)-5-hydroxy-3-pentenyl]-N-(3-methoxyphenyl)-4-methylbenzenesulfonamide

Base Information

Chemical Name:N-[(3E)-5-hydroxy-3-pentenyl]-N-(3-methoxyphenyl)-4-methylbenzenesulfonamide
CAS No.:1431116-04-9
Molecular Formula:C₁₉H₂₃NO₄S
Molecular Weight:361.462
Hs Code.:

Synonyms:N-[(3E)-5-hydroxy-3-pentenyl]-N-(3-methoxyphenyl)-4-methylbenzenesulfonamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-[(3E)-5-hydroxy-3-pentenyl]-N-(3-methoxyphenyl)-4-methylbenzenesulfonamide

Chemical Property:

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Technology Process of N-[(3E)-5-hydroxy-3-pentenyl]-N-(3-methoxyphenyl)-4-methylbenzenesulfonamide

There total 5 articles about N-[(3E)-5-hydroxy-3-pentenyl]-N-(3-methoxyphenyl)-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:

Reference yield: 85.0%

: 1431115-98-8
methyl (2E)-5-[N-(3-methoxyphenyl)-4-methylphenylsulfonamido]-2-pentenoate

: 1431116-04-9
N-[(3E)-5-hydroxy-3-pentenyl]-N-(3-methoxyphenyl)-4-methylbenzenesulfonamide

Guidance literature:: With diisobutylaluminium hydride; In dichloromethane; toluene; at 78 ℃; for 1h; Inert atmosphere;
DOI:10.1016/j.tet.2013.03.012

Reference yield:

: 58750-87-1
N-tosyl-m-anisidine

: 1431116-04-9
N-[(3E)-5-hydroxy-3-pentenyl]-N-(3-methoxyphenyl)-4-methylbenzenesulfonamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydride / N,N-dimethyl-formamide / 0.5 h / 0 °C

2.1: 9-bora-bicyclo[3.3.1]nonane / tetrahydrofuran / 20 h / 0 - 20 °C

2.2: 0.5 h / 0 °C

3.1: Dess-Martin periodane / dichloromethane / 1 h / 0 °C / Inert atmosphere

4.1: dichloromethane / 2 h / 20 °C / Inert atmosphere

5.1: diisobutylaluminium hydride / dichloromethane; toluene / 1 h / 78 °C / Inert atmosphere

With sodium hydride; diisobutylaluminium hydride; Dess-Martin periodane; 9-bora-bicyclo[3.3.1]nonane; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; toluene; 3.1: |Dess-Martin Oxidation / 4.1: |Wittig Olefination;
DOI:10.1016/j.tet.2013.03.012

Reference yield:

: 1431115-86-4
N-allyl-N-(3-methoxyphenyl)-4-methylbenzenesulfonamide

: 1431116-04-9
N-[(3E)-5-hydroxy-3-pentenyl]-N-(3-methoxyphenyl)-4-methylbenzenesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: 9-bora-bicyclo[3.3.1]nonane / tetrahydrofuran / 20 h / 0 - 20 °C

1.2: 0.5 h / 0 °C

2.1: Dess-Martin periodane / dichloromethane / 1 h / 0 °C / Inert atmosphere

3.1: dichloromethane / 2 h / 20 °C / Inert atmosphere

4.1: diisobutylaluminium hydride / dichloromethane; toluene / 1 h / 78 °C / Inert atmosphere

With diisobutylaluminium hydride; Dess-Martin periodane; 9-bora-bicyclo[3.3.1]nonane; In tetrahydrofuran; dichloromethane; toluene; 2.1: |Dess-Martin Oxidation / 3.1: |Wittig Olefination;
DOI:10.1016/j.tet.2013.03.012