(1S,2R)-{1-[(tert-butoxy)methyl]-2-cyclopent-1-enyl-2-hydroxyethyl}[(2,4,6-trimethylphenyl)sulfonyl]amine

Base Information

Chemical Name:(1S,2R)-{1-[(tert-butoxy)methyl]-2-cyclopent-1-enyl-2-hydroxyethyl}[(2,4,6-trimethylphenyl)sulfonyl]amine
CAS No.:462653-07-2
Molecular Formula:C₂₁H₃₃NO₄S
Molecular Weight:395.563
Hs Code.:

Synonyms:(1S,2R)-{1-[(tert-butoxy)methyl]-2-cyclopent-1-enyl-2-hydroxyethyl}[(2,4,6-trimethylphenyl)sulfonyl]amine

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Chemical Property of (1S,2R)-{1-[(tert-butoxy)methyl]-2-cyclopent-1-enyl-2-hydroxyethyl}[(2,4,6-trimethylphenyl)sulfonyl]amine

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Technology Process of (1S,2R)-{1-[(tert-butoxy)methyl]-2-cyclopent-1-enyl-2-hydroxyethyl}[(2,4,6-trimethylphenyl)sulfonyl]amine

There total 4 articles about (1S,2R)-{1-[(tert-butoxy)methyl]-2-cyclopent-1-enyl-2-hydroxyethyl}[(2,4,6-trimethylphenyl)sulfonyl]amine 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:

: N-(1-tert-butoxymethyl-2-cyclopent-1-enyl-2-oxo-ethyl)-2,4,6-trimethyl-benzenesulfonamide

: 462653-07-2
(1S,2R)-{1-[(tert-butoxy)methyl]-2-cyclopent-1-enyl-2-hydroxyethyl}[(2,4,6-trimethylphenyl)sulfonyl]amine

Guidance literature:: With zinc(II) tetrahydroborate; In diethyl ether; at -78 - 0 ℃;
DOI:10.1021/jo025922u

Reference yield:

: 17497-52-8
1-iodocyclopentene

: 462653-07-2
(1S,2R)-{1-[(tert-butoxy)methyl]-2-cyclopent-1-enyl-2-hydroxyethyl}[(2,4,6-trimethylphenyl)sulfonyl]amine

Guidance literature:: Multi-step reaction with 3 steps

1.1: BuLi; ZnCl₂; LiCl / tetrahydrofuran; hexane / 1 h / -78 °C

1.2: 58 percent / diisobutylaluminum hydride / various solvents / 6 h / -78 - 0 °C

2.1: Dess-Martin periodinane / CHCl₃ / 1 h / 20 °C

3.1: 2.9 g / Zn(BH₄)2 / diethyl ether / -78 - 0 °C

With n-butyllithium; zinc(II) tetrahydroborate; Dess-Martin periodane; lithium chloride; zinc(II) chloride; In tetrahydrofuran; diethyl ether; hexane; chloroform;
DOI:10.1021/jo025922u

Reference yield:

: 3-tert-butoxy-2-(2,4,6-trimethyl-benzenesulfonylamino)-propionic acid methyl ester

: 462653-07-2
(1S,2R)-{1-[(tert-butoxy)methyl]-2-cyclopent-1-enyl-2-hydroxyethyl}[(2,4,6-trimethylphenyl)sulfonyl]amine

Guidance literature:: Multi-step reaction with 3 steps

1.1: BuLi; ZnCl₂; LiCl / tetrahydrofuran; hexane / 1 h / -78 °C

1.2: 58 percent / diisobutylaluminum hydride / various solvents / 6 h / -78 - 0 °C

2.1: Dess-Martin periodinane / CHCl₃ / 1 h / 20 °C

3.1: 2.9 g / Zn(BH₄)2 / diethyl ether / -78 - 0 °C

With n-butyllithium; zinc(II) tetrahydroborate; Dess-Martin periodane; lithium chloride; zinc(II) chloride; In tetrahydrofuran; diethyl ether; hexane; chloroform;
DOI:10.1021/jo025922u