(S)-N-(but-3-en-1-yl)-4-methyl-N-(1-(pentyloxy)allyl)benzenesulfonamide

Base Information

Chemical Name:(S)-N-(but-3-en-1-yl)-4-methyl-N-(1-(pentyloxy)allyl)benzenesulfonamide
CAS No.:1438280-00-2
Molecular Formula:C₁₉H₂₉NO₃S
Molecular Weight:351.51
Hs Code.:

Synonyms:(S)-N-(but-3-en-1-yl)-4-methyl-N-(1-(pentyloxy)allyl)benzenesulfonamide

Suppliers and Price of (S)-N-(but-3-en-1-yl)-4-methyl-N-(1-(pentyloxy)allyl)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 (S)-N-(but-3-en-1-yl)-4-methyl-N-(1-(pentyloxy)allyl)benzenesulfonamide

Chemical Property:

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Technology Process of (S)-N-(but-3-en-1-yl)-4-methyl-N-(1-(pentyloxy)allyl)benzenesulfonamide

There total 1 articles about (S)-N-(but-3-en-1-yl)-4-methyl-N-(1-(pentyloxy)allyl)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: 99.0%

: 10285-80-0
N-tosyl-3-butenylamine

: 166319-26-2
1-(propa-1,2-dien-1-yloxy)pentane

: 1438280-00-2
(S)-N-(but-3-en-1-yl)-4-methyl-N-(1-(pentyloxy)allyl)benzenesulfonamide

Guidance literature:: With palladium diacetate; triethylamine; (1R,2R)-(+)-1,2-diaminocyclohexane-N,N’-bis(2-diphenylphosphino-1-naphthoyl); In dichloromethane; at 20 ℃; for 18h; Inert atmosphere;
DOI:10.1002/anie.201206967

Reference yield: 91.0%

: 1438280-00-2
(S)-N-(but-3-en-1-yl)-4-methyl-N-(1-(pentyloxy)allyl)benzenesulfonamide

: 1438279-63-0
(S)-6-(pentyloxy)-1-tosyl-1,2,3,6-tetrahydropyridine

Guidance literature:: With Grubbs catalyst first generation; In dichloromethane; at 20 ℃; for 1h; Inert atmosphere;
DOI:10.1002/anie.201206967

Reference yield:

: 1438280-00-2
(S)-N-(but-3-en-1-yl)-4-methyl-N-(1-(pentyloxy)allyl)benzenesulfonamide

: 1438279-74-3
(2S,3R,4R)-2-(pentyloxy)-1-tosylpiperidine-3,4-diol

Guidance literature:: Multi-step reaction with 2 steps

1: Grubbs catalyst first generation / dichloromethane / 1 h / 20 °C / Inert atmosphere

2: 4-methyl-2-morpholinone; osmium(VIII) oxide / acetone; tetrahydrofuran; water / 0 - 20 °C / Inert atmosphere

With Grubbs catalyst first generation; 4-methyl-2-morpholinone; osmium(VIII) oxide; In tetrahydrofuran; dichloromethane; water; acetone;
DOI:10.1002/anie.201206967