4-[4-(4-chlorophenyl)piperidin-1-yl]-1-(6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)butan-1-one

Base Information

Chemical Name:4-[4-(4-chlorophenyl)piperidin-1-yl]-1-(6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)butan-1-one
CAS No.:1345688-38-1
Molecular Formula:C₂₆H₃₂ClNO
Molecular Weight:409.999
Hs Code.:

Synonyms:4-[4-(4-chlorophenyl)piperidin-1-yl]-1-(6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)butan-1-one

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Chemical Property of 4-[4-(4-chlorophenyl)piperidin-1-yl]-1-(6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)butan-1-one

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Technology Process of 4-[4-(4-chlorophenyl)piperidin-1-yl]-1-(6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)butan-1-one

There total 5 articles about 4-[4-(4-chlorophenyl)piperidin-1-yl]-1-(6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)butan-1-one 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: 51.0%

: 74422-44-9
4-chloro-1-(6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)butan-1-one

: 6652-06-8
4-(4-chlorophenyl)-1,2,3,6-tetrahydropiperidine hydrochloride

: 1345688-38-1
4-[4-(4-chlorophenyl)piperidin-1-yl]-1-(6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)butan-1-one

Guidance literature:: With potassium carbonate; N-ethyl-N,N-diisopropylamine; potassium iodide; In N,N-dimethyl-formamide; at 60 ℃; for 16h;
DOI:10.1016/j.bmc.2011.09.007

Reference yield:

: 1075-16-7
6,7,8,9-tetrahydro-5H-benzo[7]annulene

: 1345688-38-1
4-[4-(4-chlorophenyl)piperidin-1-yl]-1-(6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)butan-1-one

Guidance literature:: Multi-step reaction with 2 steps

1: aluminum (III) chloride / Nitroethane / 2 h / 20 °C

2: potassium carbonate; N-ethyl-N,N-diisopropylamine; potassium iodide / N,N-dimethyl-formamide / 16 h / 60 °C

With aluminum (III) chloride; potassium carbonate; N-ethyl-N,N-diisopropylamine; potassium iodide; In Nitroethane; N,N-dimethyl-formamide; 1: Friedel-Crafts acylation;
DOI:10.1016/j.bmc.2011.09.007

Reference yield:

: 35550-94-8,65915-63-1,79416-49-2,138381-73-4
1-benzosuberol

: 1345688-38-1
4-[4-(4-chlorophenyl)piperidin-1-yl]-1-(6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)butan-1-one

Guidance literature:: Multi-step reaction with 4 steps

1: toluene-4-sulfonic acid / toluene / 16 h / Reflux

2: 5%-palladium/activated carbon; hydrogen / ethanol / 48 h / 20 °C

3: aluminum (III) chloride / Nitroethane / 2 h / 20 °C

4: potassium carbonate; N-ethyl-N,N-diisopropylamine; potassium iodide / N,N-dimethyl-formamide / 16 h / 60 °C

With aluminum (III) chloride; 5%-palladium/activated carbon; hydrogen; potassium carbonate; toluene-4-sulfonic acid; N-ethyl-N,N-diisopropylamine; potassium iodide; In Nitroethane; ethanol; N,N-dimethyl-formamide; toluene; 3: Friedel-Crafts acylation;
DOI:10.1016/j.bmc.2011.09.007