N-[(1R)-2-hydroxy-1-phenylethyl]-N-[(1S)-1-(tributylstannyl)pentyl]benzenesulfonamide

Base Information

Chemical Name:N-[(1R)-2-hydroxy-1-phenylethyl]-N-[(1S)-1-(tributylstannyl)pentyl]benzenesulfonamide
CAS No.:1175712-09-0
Molecular Formula:C₃₁H₅₁NO₃SSn
Molecular Weight:636.527
Hs Code.:

Synonyms:N-[(1R)-2-hydroxy-1-phenylethyl]-N-[(1S)-1-(tributylstannyl)pentyl]benzenesulfonamide

Suppliers and Price of N-[(1R)-2-hydroxy-1-phenylethyl]-N-[(1S)-1-(tributylstannyl)pentyl]benzenesulfonamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of N-[(1R)-2-hydroxy-1-phenylethyl]-N-[(1S)-1-(tributylstannyl)pentyl]benzenesulfonamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of N-[(1R)-2-hydroxy-1-phenylethyl]-N-[(1S)-1-(tributylstannyl)pentyl]benzenesulfonamide

There total 3 articles about N-[(1R)-2-hydroxy-1-phenylethyl]-N-[(1S)-1-(tributylstannyl)pentyl]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: 91.0%

: 109-72-8,29786-93-4
n-butyllithium

: 1175711-95-1,1175711-99-5
(2S,4R)-4-phenyl-3-(benzenesulfonyl)-2-(tributylstannyl)-1,3-oxazolidine

: 1175712-09-0
N-[(1R)-2-hydroxy-1-phenylethyl]-N-[(1S)-1-(tributylstannyl)pentyl]benzenesulfonamide

Guidance literature:: n-butyllithium; With copper(l) iodide; In diethyl ether; at -78 - -50 ℃; for 0.5h;

(2S,4R)-4-phenyl-3-(benzenesulfonyl)-2-(tributylstannyl)-1,3-oxazolidine; With boron trifluoride diethyl etherate; In diethyl ether; at -78 ℃; for 2h; optical yield given as %de; stereoselective reaction;
DOI:10.1021/ol300003f

Reference yield:

: 1015843-40-9
N-[(1R)-2-hydroxy-1-phenylethyl]benzenesulfonamide

: 1175712-09-0
N-[(1R)-2-hydroxy-1-phenylethyl]-N-[(1S)-1-(tributylstannyl)pentyl]benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: camphor-10-sulfonic acid; toluene-4-sulfonic acid / toluene / Reflux

2.1: copper(l) iodide / diethyl ether / 0.5 h / -78 - -50 °C

2.2: 2 h / -78 °C

With copper(l) iodide; camphor-10-sulfonic acid; toluene-4-sulfonic acid; In diethyl ether; toluene;
DOI:10.1021/ol300003f

Reference yield:

: 79411-58-8
diethoxymethyltributylstannane

: 1175712-09-0
N-[(1R)-2-hydroxy-1-phenylethyl]-N-[(1S)-1-(tributylstannyl)pentyl]benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: camphor-10-sulfonic acid; toluene-4-sulfonic acid / toluene / Reflux

2.1: copper(l) iodide / diethyl ether / 0.5 h / -78 - -50 °C

2.2: 2 h / -78 °C

With copper(l) iodide; camphor-10-sulfonic acid; toluene-4-sulfonic acid; In diethyl ether; toluene;
DOI:10.1021/ol300003f