1-Benzyl-6-methoxy-2-phenyl-1,2,3,4-tetrahydroisoquinoline

Base Information

Chemical Name:1-Benzyl-6-methoxy-2-phenyl-1,2,3,4-tetrahydroisoquinoline
CAS No.:96719-52-7
Molecular Formula:C₂₃H₂₃NO
Molecular Weight:329.442
Hs Code.:
DSSTox Substance ID:DTXSID20914372

Synonyms:96719-52-7;SCHEMBL6713459;DTXSID20914372;1-benzyl-6-methoxy-2-phenyl-1,2,3,4-tetrahydroisoquinoline;1,2,3,4-Tetrahydro-6-methoxy-1-(2-methylyphenyl)-2-phenylisoquinoline;Isoquinoline, 1,2,3,4-tetrahydro-6-methoxy-1-(2-methylyphenyl)-2-phenyl-

Suppliers and Price of 1-Benzyl-6-methoxy-2-phenyl-1,2,3,4-tetrahydroisoquinoline

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of 1-Benzyl-6-methoxy-2-phenyl-1,2,3,4-tetrahydroisoquinoline

Chemical Property:

XLogP3:5.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:329.177964357
Heavy Atom Count:25
Complexity:399

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC2=C(C=C1)C(N(CC2)C3=CC=CC=C3)CC4=CC=CC=C4

Technology Process of 1-Benzyl-6-methoxy-2-phenyl-1,2,3,4-tetrahydroisoquinoline

There total 5 articles about 1-Benzyl-6-methoxy-2-phenyl-1,2,3,4-tetrahydroisoquinoline 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:

: 1798-09-0
m-methoxyphenylacetic acid

: 96719-52-7
6-Methoxy-2-phenyl-1-o-tolyl-1,2,3,4-tetrahydro-isoquinoline

Guidance literature:: Multi-step reaction with 6 steps

1: SOCl₂ / benzene / 1 h / Heating

2: diethyl ether / Ambient temperature

3: 74 percent / LAH / dioxane; diethyl ether

4: 1.) SOCl₂ / 1.) benzene, reflux, 2.) ether, r.t.

5: 1.) POCl₃, 2.) KI / 1.) reflux, 2.) H₂O

6: NaBH₄ / methanol

With sodium tetrahydroborate; lithium aluminium tetrahydride; thionyl chloride; potassium iodide; trichlorophosphate; In 1,4-dioxane; methanol; diethyl ether; benzene;

Reference yield:

: 51009-27-9
[2-(3-Methoxy-phenyl)-ethyl]-phenyl-amine

: 96719-52-7
6-Methoxy-2-phenyl-1-o-tolyl-1,2,3,4-tetrahydro-isoquinoline

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) SOCl₂ / 1.) benzene, reflux, 2.) ether, r.t.

2: 1.) POCl₃, 2.) KI / 1.) reflux, 2.) H₂O

3: NaBH₄ / methanol

With sodium tetrahydroborate; thionyl chloride; potassium iodide; trichlorophosphate; In methanol;

Reference yield:

: 85274-96-0
2-(3-Methoxy-phenyl)-N-phenyl-acetamide

: 96719-52-7
6-Methoxy-2-phenyl-1-o-tolyl-1,2,3,4-tetrahydro-isoquinoline

Guidance literature:: Multi-step reaction with 4 steps

1: 74 percent / LAH / dioxane; diethyl ether

2: 1.) SOCl₂ / 1.) benzene, reflux, 2.) ether, r.t.

3: 1.) POCl₃, 2.) KI / 1.) reflux, 2.) H₂O

4: NaBH₄ / methanol

With sodium tetrahydroborate; lithium aluminium tetrahydride; thionyl chloride; potassium iodide; trichlorophosphate; In 1,4-dioxane; methanol; diethyl ether;