2-{4-[4-(1-Piperidin-1-yl-cyclohexyl)-phenyl]-butyl}-isoindole-1,3-dione

Base Information

Chemical Name:2-{4-[4-(1-Piperidin-1-yl-cyclohexyl)-phenyl]-butyl}-isoindole-1,3-dione
CAS No.:77415-88-4
Molecular Formula:C₂₉H₃₆N₂O₂
Molecular Weight:444.617
Hs Code.:

Synonyms:2-{4-[4-(1-Piperidin-1-yl-cyclohexyl)-phenyl]-butyl}-isoindole-1,3-dione

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Chemical Property of 2-{4-[4-(1-Piperidin-1-yl-cyclohexyl)-phenyl]-butyl}-isoindole-1,3-dione

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Technology Process of 2-{4-[4-(1-Piperidin-1-yl-cyclohexyl)-phenyl]-butyl}-isoindole-1,3-dione

There total 5 articles about 2-{4-[4-(1-Piperidin-1-yl-cyclohexyl)-phenyl]-butyl}-isoindole-1,3-dione 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%

: 77415-84-0
(E)-4-<1-(4-Phthalimido-1-butenyl)>phencyclidine

: 77415-88-4
2-{4-[4-(1-Piperidin-1-yl-cyclohexyl)-phenyl]-butyl}-isoindole-1,3-dione

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethanol; for 4h; under 2327.2 Torr;
DOI:10.1021/jo00326a033

Reference yield:

: 2201-33-4
4-Bromophencyclidine

: 77415-88-4
2-{4-[4-(1-Piperidin-1-yl-cyclohexyl)-phenyl]-butyl}-isoindole-1,3-dione

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) butyllithium, 2.) iodine / 1.) THF, -78 deg C, 2.)

2: 83 percent / triethylamine, tri-o-tolylphosphine / palladium acetate / acetonitrile / 100 °C

3: 84 percent / H₂ / 5percent Pd/C / ethanol / 4 h / 2327.2 Torr

With n-butyllithium; hydrogen; iodine; triethylamine; tris-(o-tolyl)phosphine; palladium on activated charcoal; palladium diacetate; In ethanol; acetonitrile;
DOI:10.1021/jo00326a033

Reference yield:

: 3867-15-0
1-piperidinocyclohexylcarbonitrile

: 77415-88-4
2-{4-[4-(1-Piperidin-1-yl-cyclohexyl)-phenyl]-butyl}-isoindole-1,3-dione

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) Mg, 2.) / 1.) ether, benzene, reflux, 2.) reflux, 4 h

2: 83 percent / triethylamine, tri-o-tolylphosphine / palladium acetate / acetonitrile / 100 °C

3: 84 percent / H₂ / 5percent Pd/C / ethanol / 4 h / 2327.2 Torr

With hydrogen; magnesium; triethylamine; tris-(o-tolyl)phosphine; palladium on activated charcoal; palladium diacetate; In ethanol; acetonitrile;
DOI:10.1021/jo00326a033