(R)-N-[(2-hydroxynaphthalen-1-yl)(phenyl)methyl]-4-methylbenzenesulfonamide

Base Information

Chemical Name:(R)-N-[(2-hydroxynaphthalen-1-yl)(phenyl)methyl]-4-methylbenzenesulfonamide
CAS No.:1152316-62-5
Molecular Formula:C₂₄H₂₁NO₃S
Molecular Weight:403.502
Hs Code.:

Synonyms:(R)-N-[(2-hydroxynaphthalen-1-yl)(phenyl)methyl]-4-methylbenzenesulfonamide

Suppliers and Price of (R)-N-[(2-hydroxynaphthalen-1-yl)(phenyl)methyl]-4-methylbenzenesulfonamide

Supply Marketing:

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

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Chemical Property of (R)-N-[(2-hydroxynaphthalen-1-yl)(phenyl)methyl]-4-methylbenzenesulfonamide

Chemical Property:

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Technology Process of (R)-N-[(2-hydroxynaphthalen-1-yl)(phenyl)methyl]-4-methylbenzenesulfonamide

There total 2 articles about (R)-N-[(2-hydroxynaphthalen-1-yl)(phenyl)methyl]-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: 90.0%

: 51608-60-7
phenyl N-tosyl imine

: 135-19-3
β-naphthol

: 1152316-62-5
(R)-N-[(2-hydroxynaphthalen-1-yl)(phenyl)methyl]-4-methylbenzenesulfonamide

Guidance literature:: With C₄₅H₄₈N₂O₃Zn₂; In toluene; at 30 ℃; for 48h; optical yield given as %ee; enantioselective reaction; Inert atmosphere;
DOI:10.1055/s-0029-1219390

Reference yield:

: 51608-60-7
phenyl N-tosyl imine

: 135-19-3
β-naphthol

: 1152316-62-5
(R)-N-[(2-hydroxynaphthalen-1-yl)(phenyl)methyl]-4-methylbenzenesulfonamide

: 1290137-43-7
(S)-N-[(2-hydroxynaphthalen-1-yl)(phenyl)methyl]-4-methylbenzenesulfonamide

Guidance literature:: With C₄₅H₄₈N₂O₃Zn₂; In toluene; at 30 ℃; for 48h; optical yield given as %ee; enantioselective reaction; Inert atmosphere;
DOI:10.1055/s-0029-1219390