3,3-Diethoxy-1-(4-phenylcyclohex-3-en-1-yl)propan-1-one

Base Information

Chemical Name:3,3-Diethoxy-1-(4-phenylcyclohex-3-en-1-yl)propan-1-one
CAS No.:88522-09-2
Molecular Formula:C19H26O3
Molecular Weight:302.414
Hs Code.:
DSSTox Substance ID:DTXSID50523315

Synonyms:88522-09-2;DTXSID50523315;3,3-Diethoxy-1-([2,3,4,5-tetrahydro[1,1'-biphenyl]]-4-yl)propan-1-one

Suppliers and Price of 3,3-Diethoxy-1-(4-phenylcyclohex-3-en-1-yl)propan-1-one

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
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price

Total 2 raw suppliers

Chemical Property of 3,3-Diethoxy-1-(4-phenylcyclohex-3-en-1-yl)propan-1-one

Chemical Property:

XLogP3:3.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:8
Exact Mass:302.18819469
Heavy Atom Count:22
Complexity:363

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCOC(CC(=O)C1CCC(=CC1)C2=CC=CC=C2)OCC

Technology Process of 3,3-Diethoxy-1-(4-phenylcyclohex-3-en-1-yl)propan-1-one

There total 3 articles about 3,3-Diethoxy-1-(4-phenylcyclohex-3-en-1-yl)propan-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: 100.0%

: 21181-44-2
1-(2,3,4,5-tetrahydro-[1,1′-biphenyl]-4-yl)ethan-1-one

: 88522-09-2
β-diethoxyethyl 4-phenylcyclohex-3-enyl ketone

Guidance literature:

Reference yield:

: 88522-07-0
4-Phenyl-cyclohex-3-enecarbonyl chloride

: 88522-09-2
β-diethoxyethyl 4-phenylcyclohex-3-enyl ketone

Guidance literature:: Multi-step reaction with 2 steps

1: 2.) conc. H₂SO₄, aq. AcOH / 1.) Et₂O, 0 deg C to RT, 14 h, 2.) reflux, 7 h

2: 1.) Et₂O*BF₃, 2.) N,N-diisopropyl ethylamine / 1.) CH₂Cl₂, 0 deg C, 15 min, 2.) CH₂Cl₂, -20 deg C to -10 deg C, 2 h

With sulfuric acid; boron trifluoride diethyl etherate; acetic acid; N-ethyl-N,N-diisopropylamine;
DOI:10.1021/jo00225a054

Reference yield:

: 21181-44-2
1-(2,3,4,5-tetrahydro-[1,1′-biphenyl]-4-yl)ethan-1-one

: 122-51-0
orthoformic acid triethyl ester

: 88522-09-2
β-diethoxyethyl 4-phenylcyclohex-3-enyl ketone

Guidance literature:: With boron trifluoride diethyl etherate; N-ethyl-N,N-diisopropylamine; Yield given. Multistep reaction; 1.) CH₂Cl₂, 0 deg C, 15 min, 2.) CH₂Cl₂, -20 deg C to -10 deg C, 2 h;
DOI:10.1021/jo00225a054