N-[7-benzo[1,3]dioxol-5-yl-1-(toluene-4-sulfonylmethyl)-hept-1-enyl]-N-(2-iodo-phenyl)-formamide

Base Information

Chemical Name:N-[7-benzo[1,3]dioxol-5-yl-1-(toluene-4-sulfonylmethyl)-hept-1-enyl]-N-(2-iodo-phenyl)-formamide
CAS No.:474452-42-1
Molecular Formula:C₂₉H₃₀INO₅S
Molecular Weight:631.531
Hs Code.:

<i>N</i>-[7-benzo[1,3]dioxol-5-yl-1-(toluene-4-sulfonylmethyl)-hept-1-enyl]-<i>N</i>-(2-iodo-phenyl)-formamide

Synonyms:N-[7-benzo[1,3]dioxol-5-yl-1-(toluene-4-sulfonylmethyl)-hept-1-enyl]-N-(2-iodo-phenyl)-formamide

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Chemical Property of N-[7-benzo[1,3]dioxol-5-yl-1-(toluene-4-sulfonylmethyl)-hept-1-enyl]-N-(2-iodo-phenyl)-formamide

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Technology Process of N-[7-benzo[1,3]dioxol-5-yl-1-(toluene-4-sulfonylmethyl)-hept-1-enyl]-N-(2-iodo-phenyl)-formamide

There total 8 articles about N-[7-benzo[1,3]dioxol-5-yl-1-(toluene-4-sulfonylmethyl)-hept-1-enyl]-N-(2-iodo-phenyl)-formamide 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: 79.0%

: 10113-39-0
N-formyl-2-iodoaniline

: 474452-37-4
4-[8-(p-toluenesulfonyl)-7-octynyl]-1,2-(methylenedioxy)benzene

: 474452-42-1
N-[7-benzo[1,3]dioxol-5-yl-1-(toluene-4-sulfonylmethyl)-hept-1-enyl]-N-(2-iodo-phenyl)-formamide

Guidance literature:: With dmap; potassium carbonate; In water; N,N-dimethyl-formamide; at 20 ℃; for 48h;
DOI:10.1021/jo026595t

Reference yield:

: 2635-13-4
1,2-(methylenedioxy)-4-bromobenzene

: 474452-42-1
N-[7-benzo[1,3]dioxol-5-yl-1-(toluene-4-sulfonylmethyl)-hept-1-enyl]-N-(2-iodo-phenyl)-formamide

Guidance literature:: Multi-step reaction with 8 steps

1.1: tert-butyllithium / tetrahydrofuran; pentane / 0.42 h / -78 - -42 °C

1.2: tetrahydrofuran; pentane / -78 - 20 °C

2.1: NaI / acetone / 48 h / Heating

3.1: n-butyllithium / tetrahydrofuran; hexane / 0 - 20 °C

3.2: HMPA / tetrahydrofuran; hexane / 48 h / 20 °C

4.1: 1.38 g / tetrabutylammonium fluoride / tetrahydrofuran / 0.5 h / 20 °C

5.1: CHCl₃ / 2 h / Irradiation

6.1: m-chloroperbenzoic acid / CHCl₃ / 0.33 h

7.1: 2.70 g / MgSO₄ / benzene / 1 h / Heating

8.1: 79 percent / potassium carbonate; DMAP / dimethylformamide; H₂O / 48 h / 20 °C

With dmap; n-butyllithium; tetrabutyl ammonium fluoride; tert.-butyl lithium; magnesium sulfate; potassium carbonate; 3-chloro-benzenecarboperoxoic acid; sodium iodide; In tetrahydrofuran; hexane; chloroform; water; N,N-dimethyl-formamide; acetone; pentane; benzene;
DOI:10.1021/jo026595t

Reference yield:

: 356519-62-5
4-(7-octynyl)-1,2-(methylenedioxy)benzene

: 474452-42-1
N-[7-benzo[1,3]dioxol-5-yl-1-(toluene-4-sulfonylmethyl)-hept-1-enyl]-N-(2-iodo-phenyl)-formamide

Guidance literature:: Multi-step reaction with 4 steps

1: CHCl₃ / 2 h / Irradiation

2: m-chloroperbenzoic acid / CHCl₃ / 0.33 h

3: 2.70 g / MgSO₄ / benzene / 1 h / Heating

4: 79 percent / potassium carbonate; DMAP / dimethylformamide; H₂O / 48 h / 20 °C

With dmap; magnesium sulfate; potassium carbonate; 3-chloro-benzenecarboperoxoic acid; In chloroform; water; N,N-dimethyl-formamide; benzene;
DOI:10.1021/jo026595t