N-allyl-N-[2-benzyloxy-1-(2-hydroxy-ethyl)-butyl]-4-methyl-benzenesulfonamide

Base Information

Chemical Name:N-allyl-N-[2-benzyloxy-1-(2-hydroxy-ethyl)-butyl]-4-methyl-benzenesulfonamide
CAS No.:916588-62-0
Molecular Formula:C₂₃H₃₁NO₄S
Molecular Weight:417.569
Hs Code.:

<i>N</i>-allyl-<i>N</i>-[2-benzyloxy-1-(2-hydroxy-ethyl)-butyl]-4-methyl-benzenesulfonamide

Synonyms:N-allyl-N-[2-benzyloxy-1-(2-hydroxy-ethyl)-butyl]-4-methyl-benzenesulfonamide

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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-allyl-N-[2-benzyloxy-1-(2-hydroxy-ethyl)-butyl]-4-methyl-benzenesulfonamide

Chemical Property:

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Technology Process of N-allyl-N-[2-benzyloxy-1-(2-hydroxy-ethyl)-butyl]-4-methyl-benzenesulfonamide

There total 4 articles about N-allyl-N-[2-benzyloxy-1-(2-hydroxy-ethyl)-butyl]-4-methyl-benzenesulfonamide 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: 99.0%

: 916588-55-1
N-allyl-N-{2-benzyloxy-1-[2-(tert-butyldimethylsilanyloxy)ethyl]butyl}-4-methylbenzenesulfonamide

: 916588-62-0
N-allyl-N-[2-benzyloxy-1-(2-hydroxy-ethyl)-butyl]-4-methyl-benzenesulfonamide

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 20 ℃; for 2h;
DOI:10.1016/j.tet.2006.09.004

Reference yield:

: 916588-54-0
4-benzyloxy-3-[(4-methylphenyl)sulfonylamino]hexan-1-ol

: 916588-62-0
N-allyl-N-[2-benzyloxy-1-(2-hydroxy-ethyl)-butyl]-4-methyl-benzenesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: 96 percent / imidazole / dimethylformamide / 2 h / 20 °C

2: 97 percent / sodium hydride / dimethylformamide

3: 99 percent / tetra-n-butylammonium fluoride / tetrahydrofuran / 2 h / 20 °C

With 1H-imidazole; tetrabutyl ammonium fluoride; sodium hydride; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1016/j.tet.2006.09.004

Reference yield:

: 916588-60-8
(S)-4-((R)-1-Benzyloxy-propyl)-3-(toluene-4-sulfonyl)-[1,3]oxazinan-6-one

: 916588-62-0
N-allyl-N-[2-benzyloxy-1-(2-hydroxy-ethyl)-butyl]-4-methyl-benzenesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1: 94 percent / lithium aluminum hydride / tetrahydrofuran / 0 - 20 °C

2: 96 percent / imidazole / dimethylformamide / 2 h / 20 °C

3: 97 percent / sodium hydride / dimethylformamide

4: 99 percent / tetra-n-butylammonium fluoride / tetrahydrofuran / 2 h / 20 °C

With 1H-imidazole; lithium aluminium tetrahydride; tetrabutyl ammonium fluoride; sodium hydride; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1016/j.tet.2006.09.004