(3S)-2,5-Dimethyl-3--1-hexene

Base Information

Chemical Name:(3S)-2,5-Dimethyl-3--1-hexene
CAS No.:150062-22-9
Molecular Formula:C₂₃H₃₁NO₃S
Molecular Weight:401.57
Hs Code.:

(3S)-2,5-Dimethyl-3-<N-(4-methoxybenzyl)-N-tosylamino>-1-hexene

Synonyms:(3S)-2,5-Dimethyl-3--1-hexene

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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 (3S)-2,5-Dimethyl-3--1-hexene

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Technology Process of (3S)-2,5-Dimethyl-3--1-hexene

There total 5 articles about (3S)-2,5-Dimethyl-3--1-hexene 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: 92.0%

: 2746-25-0
p-Methoxybenzyl bromide

: 127597-99-3
(3S)-2,5-Dimethyl-3-(N-tosylamino)-1-hexene

: 150062-22-9
(3S)-2,5-Dimethyl-3--1-hexene

Guidance literature:: With potassium carbonate; tetra-(n-butyl)ammonium iodide; In acetone; at 25 ℃; for 24h;
DOI:10.1021/jo00069a052

Reference yield:

: 1220-80-0,67368-40-5,150614-61-2
(S)-4-methyl-2-(toluene-4-sulfonamido)pentanoic acid

: 150062-22-9
(3S)-2,5-Dimethyl-3--1-hexene

Guidance literature:: Multi-step reaction with 3 steps

1: 53 percent / TMEDA / tetrahydrofuran / 1.) -78 deg C, 1 h, 2.) 25 deg C, 2 h

2: 1.) KN(TMS)2 / 1.) benzene, 0 to 25 deg C, 25 min, 2.) reflux, 4 h

3: 92 percent / K₂CO₃ / Bu₄NI / acetone / 24 h / 25 °C

With N,N,N,N,-tetramethylethylenediamine; potassium hexamethylsilazane; potassium carbonate; tetra-(n-butyl)ammonium iodide; In tetrahydrofuran; acetone;
DOI:10.1021/jo00069a052

Reference yield:

: 61-90-5,21675-61-6,25248-98-0,70-45-1
L-leucine

: 150062-22-9
(3S)-2,5-Dimethyl-3--1-hexene

Guidance literature:: Multi-step reaction with 4 steps

2: 53 percent / TMEDA / tetrahydrofuran / 1.) -78 deg C, 1 h, 2.) 25 deg C, 2 h

3: 1.) KN(TMS)2 / 1.) benzene, 0 to 25 deg C, 25 min, 2.) reflux, 4 h

4: 92 percent / K₂CO₃ / Bu₄NI / acetone / 24 h / 25 °C

With N,N,N,N,-tetramethylethylenediamine; potassium hexamethylsilazane; potassium carbonate; tetra-(n-butyl)ammonium iodide; In tetrahydrofuran; acetone;
DOI:10.1021/jo00069a052