(Z)-N-(4-hydroxypent-2-enyl)-4-methyl-N-(3-phenylprop-2-ynyl)benzenesulfonamide

Base Information

Chemical Name:(Z)-N-(4-hydroxypent-2-enyl)-4-methyl-N-(3-phenylprop-2-ynyl)benzenesulfonamide
CAS No.:1240184-23-9
Molecular Formula:C₂₁H₂₃NO₃S
Molecular Weight:369.485
Hs Code.:

Synonyms:(Z)-N-(4-hydroxypent-2-enyl)-4-methyl-N-(3-phenylprop-2-ynyl)benzenesulfonamide

Suppliers and Price of (Z)-N-(4-hydroxypent-2-enyl)-4-methyl-N-(3-phenylprop-2-ynyl)benzenesulfonamide

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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 (Z)-N-(4-hydroxypent-2-enyl)-4-methyl-N-(3-phenylprop-2-ynyl)benzenesulfonamide

Chemical Property:

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Technology Process of (Z)-N-(4-hydroxypent-2-enyl)-4-methyl-N-(3-phenylprop-2-ynyl)benzenesulfonamide

There total 1 articles about (Z)-N-(4-hydroxypent-2-enyl)-4-methyl-N-(3-phenylprop-2-ynyl)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:

: C₇H₁₁BrO₂

: 305837-95-0
4-methyl-N-(3-phenylprop-2-yn-1-yl)benzenesulfonamide

: 1240184-23-9
(Z)-N-(4-hydroxypent-2-enyl)-4-methyl-N-(3-phenylprop-2-ynyl)benzenesulfonamide

Guidance literature:: C₇H₁₁BrO₂; 4-methyl-N-(3-phenylprop-2-yn-1-yl)benzenesulfonamide;

With water; potassium carbonate; In methanol;
DOI:10.1021/jo101148e

Reference yield: 71.0%

: 1240184-23-9
(Z)-N-(4-hydroxypent-2-enyl)-4-methyl-N-(3-phenylprop-2-ynyl)benzenesulfonamide

: (+/-)-(3S,4R)-3-benzoyl-4-[(E)-prop-1-en-1-yl]-1-[(4-methylphenyl)sulfonyl]pyrrolidine

Guidance literature:: With (triphenylphosphine)gold(I) chloride; silver trifluoromethanesulfonate; In dichloromethane; at 25 ℃; for 2h; stereospecific reaction; Inert atmosphere;
DOI:10.1021/jo101148e

Reference yield: 19.0%

: 1240184-23-9
(Z)-N-(4-hydroxypent-2-enyl)-4-methyl-N-(3-phenylprop-2-ynyl)benzenesulfonamide

: phenyl(4-(prop-1-enyl)-1-tosylpyrrolidin-3-yl)methanone

: phenyl(4-(prop-1-enyl)-1-tosylpyrrolidin-3-yl)methanone

: C₂₁H₂₃NO₃S

Guidance literature:: With silver hexafluoroantimonate; (triphenylphosphine)gold(I) chloride; at 85 ℃; for 0.166667h; Inert atmosphere;
DOI:10.1039/c1cc10907c