5-Benzyloxy-1-(3,4-dimethoxy-benzyl)-6-methoxy-2-methyl-1,2,3,4-tetrahydro-isoquinoline

Base Information

• Chemical Name: 5-Benzyloxy-1-(3,4-dimethoxy-benzyl)-6-methoxy-2-methyl-1,2,3,4-tetrahydro-isoquinoline
• CAS No.: 108937-25-3
• Molecular Formula: C₂₇H₃₁NO₄
• Molecular Weight: 433.547
• Mol file: 108937-25-3.mol

Synonyms:5-Benzyloxy-1-(3,4-dimethoxy-benzyl)-6-methoxy-2-methyl-1,2,3,4-tetrahydro-isoquinoline

Chemical Property of 5-Benzyloxy-1-(3,4-dimethoxy-benzyl)-6-methoxy-2-methyl-1,2,3,4-tetrahydro-isoquinoline

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 5-Benzyloxy-1-(3,4-dimethoxy-benzyl)-6-methoxy-2-methyl-1,2,3,4-tetrahydro-isoquinoline

There total 4 articles about 5-Benzyloxy-1-(3,4-dimethoxy-benzyl)-6-methoxy-2-methyl-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:

(3,4-Dimethoxyphenyl)acetic acid (93-40-3) → 5-Benzyloxy-1-(3,4-dimethoxy-benzyl)-6-methoxy-2-methyl-1,2,3,4-tetrahydro-isoquinoline (108937-25-3)

Guidance literature:

Multi-step reaction with 4 steps

1: 65 percent / 5 h / 160 °C

2: Bischler-Napieralski reaction

3: NaBH₄ / methanol

4: 2.) NaBH₄ / 1.) MeOH

With sodium tetrahydroborate; In methanol;

DOI:10.1248/cpb.34.1924

Reference yield:

2-[2-(benzyloxy)-3-methoxyphenyl]ethanamine (49818-50-0) → 5-Benzyloxy-1-(3,4-dimethoxy-benzyl)-6-methoxy-2-methyl-1,2,3,4-tetrahydro-isoquinoline (108937-25-3)

Guidance literature:

Multi-step reaction with 4 steps

1: 65 percent / 5 h / 160 °C

2: Bischler-Napieralski reaction

3: NaBH₄ / methanol

4: 2.) NaBH₄ / 1.) MeOH

With sodium tetrahydroborate; In methanol;

DOI:10.1248/cpb.34.1924

Reference yield:

(3,4-dimethoxy-phenyl)-acetic acid-(2-benzyloxy-3-methoxy-phenethylamide) (108937-07-1) → 5-Benzyloxy-1-(3,4-dimethoxy-benzyl)-6-methoxy-2-methyl-1,2,3,4-tetrahydro-isoquinoline (108937-25-3)

Guidance literature:

Multi-step reaction with 3 steps

1: Bischler-Napieralski reaction

2: NaBH₄ / methanol

3: 2.) NaBH₄ / 1.) MeOH

With sodium tetrahydroborate; In methanol;

DOI:10.1248/cpb.34.1924

upstream raw materials:

(3,4-Dimethoxyphenyl)acetic acid

2-[2-(benzyloxy)-3-methoxyphenyl]ethanamine

(3,4-dimethoxy-phenyl)-acetic acid-(2-benzyloxy-3-methoxy-phenethylamide)

5-Benzyloxy-1-(3,4-dimethoxy-benzyl)-6-methoxy-3,4-dihydro-isoquinoline; hydrochloride

Downstream raw materials:

Acetic acid 1-(3,4-dimethoxy-benzyl)-6-methoxy-2-methyl-5-oxo-1,2,3,4,5,6-hexahydro-isoquinolin-6-yl ester

1-(3,4-Dimethoxy-benzyl)-6-methoxy-2-methyl-1,2,3,4-tetrahydro-isoquinolin-5-ol