(E)-N-(6-(tert-butyldimethylsilyloxy)hex-4-enyl)-4-methylbenzenesulfonamide

Base Information

Chemical Name:(E)-N-(6-(tert-butyldimethylsilyloxy)hex-4-enyl)-4-methylbenzenesulfonamide
CAS No.:1311201-43-0
Molecular Formula:C₁₉H₃₃NO₃SSi
Molecular Weight:383.627
Hs Code.:

Synonyms:(E)-N-(6-(tert-butyldimethylsilyloxy)hex-4-enyl)-4-methylbenzenesulfonamide

Suppliers and Price of (E)-N-(6-(tert-butyldimethylsilyloxy)hex-4-enyl)-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 (E)-N-(6-(tert-butyldimethylsilyloxy)hex-4-enyl)-4-methylbenzenesulfonamide

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Technology Process of (E)-N-(6-(tert-butyldimethylsilyloxy)hex-4-enyl)-4-methylbenzenesulfonamide

There total 9 articles about (E)-N-(6-(tert-butyldimethylsilyloxy)hex-4-enyl)-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: 84.0%

: 1311201-42-9
(E)-methyl 6-(tert-butyldimethylsilyloxy)hex-4-enyl(tosyl)carbamate

: 1311201-43-0
(E)-N-(6-(tert-butyldimethylsilyloxy)hex-4-enyl)-4-methylbenzenesulfonamide

Guidance literature:: With methanol; potassium carbonate; at 25 - 28 ℃; for 1.5h; Inert atmosphere;
DOI:10.1002/anie.201100772

Reference yield:

: 1353722-74-3
(E)-5-hydroxypent-3-en-1-yl 4-methylbenzenesulfonate

: 1311201-43-0
(E)-N-(6-(tert-butyldimethylsilyloxy)hex-4-enyl)-4-methylbenzenesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1: methanol / 3 h / Inert atmosphere; Reflux

2: 1H-imidazole / dichloromethane / 0.33 h / 20 °C / Inert atmosphere

3: lithium aluminium tetrahydride / diethyl ether / 1 h / 20 °C / Inert atmosphere

4: pyridine / dichloromethane / 5 h / 20 °C / Inert atmosphere

With pyridine; 1H-imidazole; lithium aluminium tetrahydride; In methanol; diethyl ether; dichloromethane;
DOI:10.1021/ol203218d

Reference yield:

: 1353722-75-4
(E)-6-hydroxyhex-4-enenitrile

: 1311201-43-0
(E)-N-(6-(tert-butyldimethylsilyloxy)hex-4-enyl)-4-methylbenzenesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: 1H-imidazole / dichloromethane / 0.33 h / 20 °C / Inert atmosphere

2: lithium aluminium tetrahydride / diethyl ether / 1 h / 20 °C / Inert atmosphere

3: pyridine / dichloromethane / 5 h / 20 °C / Inert atmosphere

With pyridine; 1H-imidazole; lithium aluminium tetrahydride; In diethyl ether; dichloromethane;
DOI:10.1021/ol203218d