(4S,5S)-4-mesyloxymethyl-5-(4-methylsulfanylphenyl)-2-tert-butyl-oxazoline

Base Information

Chemical Name:(4S,5S)-4-mesyloxymethyl-5-(4-methylsulfanylphenyl)-2-tert-butyl-oxazoline
CAS No.:914477-60-4
Molecular Formula:C₁₆H₂₃NO₄S₂
Molecular Weight:357.495
Hs Code.:

Synonyms:(4S,5S)-4-mesyloxymethyl-5-(4-methylsulfanylphenyl)-2-tert-butyl-oxazoline

Suppliers and Price of (4S,5S)-4-mesyloxymethyl-5-(4-methylsulfanylphenyl)-2-tert-butyl-oxazoline

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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 (4S,5S)-4-mesyloxymethyl-5-(4-methylsulfanylphenyl)-2-tert-butyl-oxazoline

Chemical Property:

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Technology Process of (4S,5S)-4-mesyloxymethyl-5-(4-methylsulfanylphenyl)-2-tert-butyl-oxazoline

There total 3 articles about (4S,5S)-4-mesyloxymethyl-5-(4-methylsulfanylphenyl)-2-tert-butyl-oxazoline 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: 68.0%

: 914477-56-8
(4S,5S)-4-hydroxymethyl-5-(4-methylsulfanylphenyl)-2-tert-butyl-oxazoline

: 124-63-0
methanesulfonyl chloride

: 914477-60-4
(4S,5S)-4-mesyloxymethyl-5-(4-methylsulfanylphenyl)-2-tert-butyl-oxazoline

Guidance literature:: With triethylamine; In dichloromethane; at 0 - 20 ℃;
DOI:10.1016/j.tet.2006.08.003

Reference yield:

: 16854-32-3
(1S,2S)-(+)-thiomicamine

: 914477-60-4
(4S,5S)-4-mesyloxymethyl-5-(4-methylsulfanylphenyl)-2-tert-butyl-oxazoline

Guidance literature:: Multi-step reaction with 2 steps

1: 62 percent / chlorobenzene / 18 h / Heating

2: 68 percent / triethylamine / CH₂Cl₂ / 0 - 20 °C

With triethylamine; In dichloromethane; chlorobenzene;
DOI:10.1016/j.tet.2006.08.003

Reference yield:

: 52186-79-5
2,2-dimethyl-propionimidic acid ethyl ester

: 914477-60-4
(4S,5S)-4-mesyloxymethyl-5-(4-methylsulfanylphenyl)-2-tert-butyl-oxazoline

Guidance literature:: Multi-step reaction with 2 steps

1: 62 percent / chlorobenzene / 18 h / Heating

2: 68 percent / triethylamine / CH₂Cl₂ / 0 - 20 °C

With triethylamine; In dichloromethane; chlorobenzene;
DOI:10.1016/j.tet.2006.08.003