N-((3S,4R)-4-hydroxy-4-phenylhept-6-en-3-yl)-4-methylbenzenesulfonamide

Base Information

Chemical Name:N-((3S,4R)-4-hydroxy-4-phenylhept-6-en-3-yl)-4-methylbenzenesulfonamide
CAS No.:1261245-14-0
Molecular Formula:C₂₀H₂₅NO₃S
Molecular Weight:359.489
Hs Code.:

Synonyms:N-((3S,4R)-4-hydroxy-4-phenylhept-6-en-3-yl)-4-methylbenzenesulfonamide

Suppliers and Price of N-((3S,4R)-4-hydroxy-4-phenylhept-6-en-3-yl)-4-methylbenzenesulfonamide

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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-((3S,4R)-4-hydroxy-4-phenylhept-6-en-3-yl)-4-methylbenzenesulfonamide

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Technology Process of N-((3S,4R)-4-hydroxy-4-phenylhept-6-en-3-yl)-4-methylbenzenesulfonamide

There total 1 articles about N-((3S,4R)-4-hydroxy-4-phenylhept-6-en-3-yl)-4-methylbenzenesulfonamide 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:

: (S)-4-methyl-N-(1-oxo-1-phenylbutan-2-yl)benzenesulfonamide

: 2622-05-1
allylmagnesium bromide

: 1261245-14-0
N-((3S,4R)-4-hydroxy-4-phenylhept-6-en-3-yl)-4-methylbenzenesulfonamide

Guidance literature:: (S)-4-methyl-N-(1-oxo-1-phenylbutan-2-yl)benzenesulfonamide; allylmagnesium bromide; In tetrahydrofuran; at 0 - 20 ℃; Inert atmosphere;

With water; ammonium chloride; In tetrahydrofuran; at 20 ℃; optical yield given as %ee; diastereoselective reaction;
DOI:10.1002/adsc.201000450

Reference yield: 56.0%

: 1261245-14-0
N-((3S,4R)-4-hydroxy-4-phenylhept-6-en-3-yl)-4-methylbenzenesulfonamide

: 1261245-41-3
(2S,5S)-2-ethyl-5-methyl-3-phenyl-1-tosyl-2,5-dihydro-1H-pyrrole

Guidance literature:: With copper(II) bis(trifluoromethanesulfonate); In 1,2-dichloro-ethane; at 80 ℃; for 15h; optical yield given as %ee; enantioselective reaction; Inert atmosphere;
DOI:10.1002/adsc.201000450