1-(4-chloro-phenoxymethyl)-6,7-dimethoxy-1,2,3,4-tetrahydro-isoquinoline

Base Information

Chemical Name:1-(4-chloro-phenoxymethyl)-6,7-dimethoxy-1,2,3,4-tetrahydro-isoquinoline
CAS No.:3131-43-9
Molecular Formula:C₁₈H₂₀ClNO₃
Molecular Weight:333.815
Hs Code.:

Synonyms:1-(4-chloro-phenoxymethyl)-6,7-dimethoxy-1,2,3,4-tetrahydro-isoquinoline

Suppliers and Price of 1-(4-chloro-phenoxymethyl)-6,7-dimethoxy-1,2,3,4-tetrahydro-isoquinoline

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
Packaging
price

Total 0 raw suppliers

Chemical Property of 1-(4-chloro-phenoxymethyl)-6,7-dimethoxy-1,2,3,4-tetrahydro-isoquinoline

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 1-(4-chloro-phenoxymethyl)-6,7-dimethoxy-1,2,3,4-tetrahydro-isoquinoline

There total 5 articles about 1-(4-chloro-phenoxymethyl)-6,7-dimethoxy-1,2,3,4-tetrahydro-isoquinoline 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: 87.0%

: 3341-29-5
1-(4-chloro-phenoxymethyl)-6,7-dimethoxy-3,4-dihydro-isoquinoline

: 3131-43-9
1-(4-chloro-phenoxymethyl)-6,7-dimethoxy-1,2,3,4-tetrahydro-isoquinoline

Guidance literature:: With sodium tetrahydroborate; In methanol; for 8h; Ambient temperature;
DOI:10.1002/jhet.5570360112

Reference yield:

: 14301-31-6
2-chloro-N-(2-(3,4-dimethoxyphenyl)ethyl)acetamide

: 3131-43-9
1-(4-chloro-phenoxymethyl)-6,7-dimethoxy-1,2,3,4-tetrahydro-isoquinoline

Guidance literature:: Multi-step reaction with 3 steps

1: 94 percent / K₂CO₃ / acetonitrile / 6 h / Heating

2: 89 percent / POCl₃ / toluene / 4 h / Heating

3: 87 percent / NaBH₄ / methanol / 8 h / Ambient temperature

With sodium tetrahydroborate; potassium carbonate; trichlorophosphate; In methanol; toluene; acetonitrile;
DOI:10.1002/jhet.5570360112

Reference yield:

: 3542-33-4
(4-Chlor-phenoxy)-essigsaeure-(3,4-dimethoxy-phenaethylamid)

: 3131-43-9
1-(4-chloro-phenoxymethyl)-6,7-dimethoxy-1,2,3,4-tetrahydro-isoquinoline

Guidance literature:: Multi-step reaction with 2 steps

1: 89 percent / POCl₃ / toluene / 4 h / Heating

2: 87 percent / NaBH₄ / methanol / 8 h / Ambient temperature

With sodium tetrahydroborate; trichlorophosphate; In methanol; toluene;
DOI:10.1002/jhet.5570360112