6-benzyloxy-1-(3-benzyloxy-4,5-dimethoxyphenethyl)-7-methoxy-2-methyl-1,2,3,4-tetrahydroisoquinoline

Base Information

Chemical Name:6-benzyloxy-1-(3-benzyloxy-4,5-dimethoxyphenethyl)-7-methoxy-2-methyl-1,2,3,4-tetrahydroisoquinoline
CAS No.:156488-60-7
Molecular Formula:C₃₅H₃₉NO₅
Molecular Weight:553.698
Hs Code.:

Synonyms:6-benzyloxy-1-(3-benzyloxy-4,5-dimethoxyphenethyl)-7-methoxy-2-methyl-1,2,3,4-tetrahydroisoquinoline

Suppliers and Price of 6-benzyloxy-1-(3-benzyloxy-4,5-dimethoxyphenethyl)-7-methoxy-2-methyl-1,2,3,4-tetrahydroisoquinoline

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 6-benzyloxy-1-(3-benzyloxy-4,5-dimethoxyphenethyl)-7-methoxy-2-methyl-1,2,3,4-tetrahydroisoquinoline

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 6-benzyloxy-1-(3-benzyloxy-4,5-dimethoxyphenethyl)-7-methoxy-2-methyl-1,2,3,4-tetrahydroisoquinoline

There total 10 articles about 6-benzyloxy-1-(3-benzyloxy-4,5-dimethoxyphenethyl)-7-methoxy-2-methyl-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: 93.0%

: 6-benzyloxy-1-(3-benzyloxy-4,5-dimethoxyphenethyl)-7-methoxy-2-methyl-3,4-dihydroisoquinolinium iodide

: 156488-60-7
6-benzyloxy-1-(3-benzyloxy-4,5-dimethoxyphenethyl)-7-methoxy-2-methyl-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: With sodium tetrahydroborate; In methanol; for 2h; Ambient temperature;

Reference yield:

: 32024-15-0
3,4-dimethoxy-5-iodobenzaldehyde

: 156488-60-7
6-benzyloxy-1-(3-benzyloxy-4,5-dimethoxyphenethyl)-7-methoxy-2-methyl-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: Multi-step reaction with 9 steps

1: 76 percent / piperidine / pyridine / 2 h / Heating

2: 60.8 percent / NaOH, CuSO₄*5H₂O / H₂O / 12 h / Heating

3: 96 percent / H₂, 10percent NaOH / 10percent Pd/C / ethanol / Ambient temperature

4: 80 percent / K₂CO₃ / ethanol / 10 h / Heating

5: SOCl₂ / benzene / 1 h / Heating

6: pyridine / CHCl₃ / 4 h / Ambient temperature

7: POCl₃ / benzene / 4 h / Heating

8: benzene / 60 h / 0 °C

9: 93 percent / NaBH₄ / methanol / 2 h / Ambient temperature

With piperidine; pyridine; sodium hydroxide; sodium tetrahydroborate; thionyl chloride; hydrogen; potassium carbonate; copper(II) sulfate; trichlorophosphate; palladium on activated charcoal; In pyridine; methanol; ethanol; chloroform; water; benzene;

Reference yield:

: 5438-36-8
5-iodovaniline

: 156488-60-7
6-benzyloxy-1-(3-benzyloxy-4,5-dimethoxyphenethyl)-7-methoxy-2-methyl-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: Multi-step reaction with 10 steps

1: 97 percent / K₂CO₃ / dimethylformamide / 5 h / 100 - 120 °C

2: 76 percent / piperidine / pyridine / 2 h / Heating

3: 60.8 percent / NaOH, CuSO₄*5H₂O / H₂O / 12 h / Heating

4: 96 percent / H₂, 10percent NaOH / 10percent Pd/C / ethanol / Ambient temperature

5: 80 percent / K₂CO₃ / ethanol / 10 h / Heating

6: SOCl₂ / benzene / 1 h / Heating

7: pyridine / CHCl₃ / 4 h / Ambient temperature

8: POCl₃ / benzene / 4 h / Heating

9: benzene / 60 h / 0 °C

10: 93 percent / NaBH₄ / methanol / 2 h / Ambient temperature

With piperidine; pyridine; sodium hydroxide; sodium tetrahydroborate; thionyl chloride; hydrogen; potassium carbonate; copper(II) sulfate; trichlorophosphate; palladium on activated charcoal; In pyridine; methanol; ethanol; chloroform; water; N,N-dimethyl-formamide; benzene;