3,4-Dimethyl-2-<(Z)-6-(tetrahydro-2H-pyranyloxy)-3-hexen-1-yl>-3-cyclohexen-1-on

Base Information

Chemical Name:3,4-Dimethyl-2-<(Z)-6-(tetrahydro-2H-pyranyloxy)-3-hexen-1-yl>-3-cyclohexen-1-on
CAS No.:120385-68-4
Molecular Formula:C₁₉H₃₀O₃
Molecular Weight:306.445
Hs Code.:

Synonyms:3,4-Dimethyl-2-<(Z)-6-(tetrahydro-2H-pyranyloxy)-3-hexen-1-yl>-3-cyclohexen-1-on

Suppliers and Price of 3,4-Dimethyl-2-<(Z)-6-(tetrahydro-2H-pyranyloxy)-3-hexen-1-yl>-3-cyclohexen-1-on

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 3,4-Dimethyl-2-<(Z)-6-(tetrahydro-2H-pyranyloxy)-3-hexen-1-yl>-3-cyclohexen-1-on

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 3,4-Dimethyl-2-<(Z)-6-(tetrahydro-2H-pyranyloxy)-3-hexen-1-yl>-3-cyclohexen-1-on

There total 6 articles about 3,4-Dimethyl-2-<(Z)-6-(tetrahydro-2H-pyranyloxy)-3-hexen-1-yl>-3-cyclohexen-1-on 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:

: 104178-62-3
6-<(tetrahydro-2H-pyran-2-yl)oxy>-3-hexyn-1-ol

: 120385-68-4
3,4-Dimethyl-2-<(Z)-6-(tetrahydro-2H-pyranyloxy)-3-hexen-1-yl>-3-cyclohexen-1-on

Guidance literature:: Multi-step reaction with 5 steps

1: 94 percent / H₂, quinoline / 10percent Pd/BaSO₄ / petroleum ether / 6 h

2: 93 percent / 40percent NaOH / 5 h / 40 °C

3: 76 percent / LiBr / dimethylsulfoxide / 2 h / 70 °C

4: 1.) 15percent BuLi / 1.) n-hexane, THF, -80 deg C, 15 min, 2.) HMPA, -70 deg C

5: 3N HCl / diethyl ether / 0.03 h / 0 °C

With quinoline; hydrogenchloride; sodium hydroxide; n-butyllithium; hydrogen; lithium bromide; Pd-BaSO₄; In diethyl ether; dimethyl sulfoxide; Petroleum ether;

Reference yield:

: 120385-61-7
4-<2-(Diethylamino)ethoxy>-1,2-dimethyl-3-<(Z)-6-(tetrahydro-2H-pyranyloxy)-3-hexen-1-yl>-1,4-cyclohexadien

: 120385-62-8
3,4-Dimethyl-2-<(Z)-6-(tetrahydro-2H-pyranyloxy)-3-hexen-1-yl>-2-cyclohexen-1-on

: 120385-68-4
3,4-Dimethyl-2-<(Z)-6-(tetrahydro-2H-pyranyloxy)-3-hexen-1-yl>-3-cyclohexen-1-on

Guidance literature:: With hydrogenchloride; In diethyl ether; at 0 ℃; for 0.0333333h; Yield given. Yields of byproduct given;

Reference yield:

: 72530-35-9
<(Z)-6-(Tetrahydro-2H-pyranyloxy)-3-hexen-1-yl>-p-toluolsulfonat

: 120385-68-4
3,4-Dimethyl-2-<(Z)-6-(tetrahydro-2H-pyranyloxy)-3-hexen-1-yl>-3-cyclohexen-1-on

Guidance literature:: Multi-step reaction with 3 steps

1: 76 percent / LiBr / dimethylsulfoxide / 2 h / 70 °C

2: 1.) 15percent BuLi / 1.) n-hexane, THF, -80 deg C, 15 min, 2.) HMPA, -70 deg C

3: 3N HCl / diethyl ether / 0.03 h / 0 °C

With hydrogenchloride; n-butyllithium; lithium bromide; In diethyl ether; dimethyl sulfoxide;