N-tert-butyl-O-[1-(4-(mercaptomethyl)phenyl)ethyl]-N-(2-methyl-1-phenylpropyl)hydroxylamine

Base Information

Chemical Name:N-tert-butyl-O-[1-(4-(mercaptomethyl)phenyl)ethyl]-N-(2-methyl-1-phenylpropyl)hydroxylamine
CAS No.:1100759-27-0
Molecular Formula:C₂₃H₃₃NOS
Molecular Weight:371.587
Hs Code.:

Synonyms:N-tert-butyl-O-[1-(4-(mercaptomethyl)phenyl)ethyl]-N-(2-methyl-1-phenylpropyl)hydroxylamine

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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-tert-butyl-O-[1-(4-(mercaptomethyl)phenyl)ethyl]-N-(2-methyl-1-phenylpropyl)hydroxylamine

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Technology Process of N-tert-butyl-O-[1-(4-(mercaptomethyl)phenyl)ethyl]-N-(2-methyl-1-phenylpropyl)hydroxylamine

There total 5 articles about N-tert-butyl-O-[1-(4-(mercaptomethyl)phenyl)ethyl]-N-(2-methyl-1-phenylpropyl)hydroxylamine 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%

: 1100759-25-8
N-tert-butyl-O-{1-[4-(4-{1-[N-tert-butyl-N-(2-methyl-1-phenylpropyl)aminooxy] ethyl}benzyldisulfanylmethyl)phenyl]ethyl}-N-(2-methyl-1-phenylpropyl)hydroxylamine

: 1100759-27-0
N-tert-butyl-O-[1-(4-(mercaptomethyl)phenyl)ethyl]-N-(2-methyl-1-phenylpropyl)hydroxylamine

Guidance literature:: With 1,4-dithio-D,L-threitol; In N,N-dimethyl-formamide; at 60 ℃; Inert atmosphere;
DOI:10.1016/j.reactfunctpolym.2013.01.009

Reference yield:

: 6987-22-0
amino[(4-ethenylbenzyl)sulfanyl]methanaminium chloride

: 1100759-27-0
N-tert-butyl-O-[1-(4-(mercaptomethyl)phenyl)ethyl]-N-(2-methyl-1-phenylpropyl)hydroxylamine

Guidance literature:: Multi-step reaction with 4 steps

1: sodium hydroxide / N,N-dimethyl-formamide / 2 h / 20 °C / Inert atmosphere

2: sodium hydroxide / 50 °C

3: 2,2′-((1E,1′E)-(ethane-1,2-diylbis(azanylylidene))bis(methanylylidene))diphenolmanganese(II); sodium tetrahydroborate / toluene; ethanol

4: 1,4-dithio-D,L-threitol / N,N-dimethyl-formamide / 60 °C / Inert atmosphere

With sodium tetrahydroborate; 2,2′-((1E,1′E)-(ethane-1,2-diylbis(azanylylidene))bis(methanylylidene))diphenolmanganese(II); 1,4-dithio-D,L-threitol; sodium hydroxide; In ethanol; N,N-dimethyl-formamide; toluene;
DOI:10.1016/j.reactfunctpolym.2013.01.009

Reference yield:

: 6987-23-1
4-vinyl-phenyl methane thiol

: 1100759-27-0
N-tert-butyl-O-[1-(4-(mercaptomethyl)phenyl)ethyl]-N-(2-methyl-1-phenylpropyl)hydroxylamine

Guidance literature:: Multi-step reaction with 3 steps

1: sodium hydroxide / 50 °C

2: 2,2′-((1E,1′E)-(ethane-1,2-diylbis(azanylylidene))bis(methanylylidene))diphenolmanganese(II); sodium tetrahydroborate / toluene; ethanol

3: 1,4-dithio-D,L-threitol / N,N-dimethyl-formamide / 60 °C / Inert atmosphere

With sodium tetrahydroborate; 2,2′-((1E,1′E)-(ethane-1,2-diylbis(azanylylidene))bis(methanylylidene))diphenolmanganese(II); 1,4-dithio-D,L-threitol; sodium hydroxide; In ethanol; N,N-dimethyl-formamide; toluene;
DOI:10.1016/j.reactfunctpolym.2013.01.009