3-<(E)-3-(2,6,6-trimethyl-2-cyclohexen-1-ylidene)-1-methyl-1-propyl>-5-<(E)-3-(acetyloxy)-1-methyl-1-propenyl>-isoxazole

Base Information

Chemical Name:3-<(E)-3-(2,6,6-trimethyl-2-cyclohexen-1-ylidene)-1-methyl-1-propyl>-5-<(E)-3-(acetyloxy)-1-methyl-1-propenyl>-isoxazole
CAS No.:125316-32-7
Molecular Formula:C₂₂H₃₁NO₃
Molecular Weight:357.493
Hs Code.:

Synonyms:3-<(E)-3-(2,6,6-trimethyl-2-cyclohexen-1-ylidene)-1-methyl-1-propyl>-5-<(E)-3-(acetyloxy)-1-methyl-1-propenyl>-isoxazole

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Chemical Property of 3-<(E)-3-(2,6,6-trimethyl-2-cyclohexen-1-ylidene)-1-methyl-1-propyl>-5-<(E)-3-(acetyloxy)-1-methyl-1-propenyl>-isoxazole

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Technology Process of 3-<(E)-3-(2,6,6-trimethyl-2-cyclohexen-1-ylidene)-1-methyl-1-propyl>-5-<(E)-3-(acetyloxy)-1-methyl-1-propenyl>-isoxazole

There total 6 articles about 3-<(E)-3-(2,6,6-trimethyl-2-cyclohexen-1-ylidene)-1-methyl-1-propyl>-5-<(E)-3-(acetyloxy)-1-methyl-1-propenyl>-isoxazole 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: 65.0%

: 125316-31-6,130285-77-7,130285-80-2
3-<3-(2,6,6-trimethyl-1-cyclohexen-1-yl)-3-hydroxy-1-methyl-1-propyl>-5-<(E)-3-(acetyloxy)-1-methyl-1-propenyl>-isoxazole

: 125316-32-7
3-<(E)-3-(2,6,6-trimethyl-2-cyclohexen-1-ylidene)-1-methyl-1-propyl>-5-<(E)-3-(acetyloxy)-1-methyl-1-propenyl>-isoxazole

Guidance literature:: With toluene-4-sulfonic acid; In benzene; at 50 ℃; for 1.5h;
DOI:10.1016/0223-5234(90)90212-L

Reference yield:

: 23726-91-2
beta damascone

: 125316-32-7
3-<(E)-3-(2,6,6-trimethyl-2-cyclohexen-1-ylidene)-1-methyl-1-propyl>-5-<(E)-3-(acetyloxy)-1-methyl-1-propenyl>-isoxazole

Guidance literature:: Multi-step reaction with 6 steps

1: 80 percent / tetramethylguanidine / 24 h / Ambient temperature

2: 90 percent / Et₃N, phenylisocyanate / benzene / Ambient temperature

3: 85 percent / LiOH*H₂O / methanol; H₂O / 0.17 h / 0 °C

4: 66.6 percent / diisobutyl-aluminium hydride / toluene / 2 h / -78 °C

5: 70 percent / Et₃N, 4-dimethylaminopyridine / CH₂Cl₂ / 0.5 h / Ambient temperature

6: 65 percent / p-toluenesulfonic acid / benzene / 1.5 h / 50 °C

With dmap; lithium hydroxide; diisobutylaluminum hydride; 1,1,3,3-tetramethylguanidine; phenyl isocyanate; toluene-4-sulfonic acid; triethylamine; In methanol; dichloromethane; water; toluene; benzene;
DOI:10.1016/0223-5234(90)90212-L

Reference yield:

: 130285-75-5
3-methyl-4-nitro-1-(2',6',6'-trimethylcyclohex-1-en-1-yl)butan-1-one

: 125316-32-7
3-<(E)-3-(2,6,6-trimethyl-2-cyclohexen-1-ylidene)-1-methyl-1-propyl>-5-<(E)-3-(acetyloxy)-1-methyl-1-propenyl>-isoxazole

Guidance literature:: Multi-step reaction with 5 steps

1: 90 percent / Et₃N, phenylisocyanate / benzene / Ambient temperature

2: 85 percent / LiOH*H₂O / methanol; H₂O / 0.17 h / 0 °C

3: 66.6 percent / diisobutyl-aluminium hydride / toluene / 2 h / -78 °C

4: 70 percent / Et₃N, 4-dimethylaminopyridine / CH₂Cl₂ / 0.5 h / Ambient temperature

5: 65 percent / p-toluenesulfonic acid / benzene / 1.5 h / 50 °C

With dmap; lithium hydroxide; diisobutylaluminum hydride; phenyl isocyanate; toluene-4-sulfonic acid; triethylamine; In methanol; dichloromethane; water; toluene; benzene;
DOI:10.1016/0223-5234(90)90212-L