N-{(1R,2R)-1-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-2-hydroxymethyl-butyl}-4-methyl-benzenesulfonamide

Base Information

Chemical Name:N-{(1R,2R)-1-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-2-hydroxymethyl-butyl}-4-methyl-benzenesulfonamide
CAS No.:115946-41-3
Molecular Formula:C₃₀H₄₁NO₄SSi
Molecular Weight:539.811
Hs Code.:

Synonyms:N-{(1R,2R)-1-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-2-hydroxymethyl-butyl}-4-methyl-benzenesulfonamide

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Chemical Property of N-{(1R,2R)-1-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-2-hydroxymethyl-butyl}-4-methyl-benzenesulfonamide

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Technology Process of N-{(1R,2R)-1-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-2-hydroxymethyl-butyl}-4-methyl-benzenesulfonamide

There total 4 articles about N-{(1R,2R)-1-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-2-hydroxymethyl-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:

: 811-49-4
ethyllithium

: 115946-40-2
[(2S,3R)-3-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-1-(toluene-4-sulfonyl)-aziridin-2-yl]-methanol

: 115946-41-3
N-{(1R,2R)-1-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-2-hydroxymethyl-butyl}-4-methyl-benzenesulfonamide

Guidance literature:: With copper(l) iodide; In diethyl ether; at -78 ℃; for 1h; Yield given. Yields of byproduct given;
DOI:10.1016/S0040-4020(01)85849-X

Reference yield:

: 127758-12-7
(2R,3R)-(3-(2-(2,2-dimethyl-1,1-diphenyl-1-silapropoxy)ethyl)-2-oxiranyl)methan-1-ol

: 115946-41-3
N-{(1R,2R)-1-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-2-hydroxymethyl-butyl}-4-methyl-benzenesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

2: 96 percent / pyridine / -20 °C

3: 82 percent / acetic acid; H₂O / 72 h / Ambient temperature

4: CuI / diethyl ether / 1 h / -78 °C

With copper(l) iodide; In pyridine; diethyl ether; water; acetic acid;
DOI:10.1016/S0040-4020(01)85849-X

Reference yield:

: 115946-38-8
(2S,3R)-2-(tert-Butyl-dimethyl-silanyloxymethyl)-3-[2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-aziridine

: 115946-41-3
N-{(1R,2R)-1-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-2-hydroxymethyl-butyl}-4-methyl-benzenesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: 96 percent / pyridine / -20 °C

2: 82 percent / acetic acid; H₂O / 72 h / Ambient temperature

3: CuI / diethyl ether / 1 h / -78 °C

With copper(l) iodide; In pyridine; diethyl ether; water; acetic acid;
DOI:10.1016/S0040-4020(01)85849-X