Acetic acid (R)-2-(6-amino-3,4-dimethoxy-2-methyl-phenyl)-1-methyl-ethyl ester

Base Information

Chemical Name:Acetic acid (R)-2-(6-amino-3,4-dimethoxy-2-methyl-phenyl)-1-methyl-ethyl ester
CAS No.:264607-06-9
Molecular Formula:C₁₄H₂₁NO₄
Molecular Weight:267.325
Hs Code.:

Synonyms:Acetic acid (R)-2-(6-amino-3,4-dimethoxy-2-methyl-phenyl)-1-methyl-ethyl ester

Suppliers and Price of Acetic acid (R)-2-(6-amino-3,4-dimethoxy-2-methyl-phenyl)-1-methyl-ethyl ester

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 Acetic acid (R)-2-(6-amino-3,4-dimethoxy-2-methyl-phenyl)-1-methyl-ethyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of Acetic acid (R)-2-(6-amino-3,4-dimethoxy-2-methyl-phenyl)-1-methyl-ethyl ester

There total 6 articles about Acetic acid (R)-2-(6-amino-3,4-dimethoxy-2-methyl-phenyl)-1-methyl-ethyl ester 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: 86.0%

: 264607-09-2
Acetic acid (R)-2-(3,4-dimethoxy-2-methyl-6-nitro-phenyl)-1-methyl-ethyl ester

: 264607-06-9
Acetic acid (R)-2-(6-amino-3,4-dimethoxy-2-methyl-phenyl)-1-methyl-ethyl ester

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol; at 25 ℃;
DOI:10.1016/S0040-4039(99)02257-1

Reference yield:

: 4463-33-6
1,2-dimethoxy-3-methylbenzene

: 264607-06-9
Acetic acid (R)-2-(6-amino-3,4-dimethoxy-2-methyl-phenyl)-1-methyl-ethyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 96 percent / NBS / acetonitrile / 20 h / 25 °C

2: 80 percent / n-BuLi / tetrahydrofuran / -78 °C

3: tetrahydrofuran / -78 - 25 °C

4: 100 percent / Et₃N; DMAP / CH₂Cl₂ / 20 h / 25 °C

5: 87 percent / HNO₃ / acetic anhydride; acetic acid / 4 h / 0 °C

6: 86 percent / H₂ / Pd/C / methanol / 25 °C

With dmap; N-Bromosuccinimide; n-butyllithium; hydrogen; nitric acid; triethylamine; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; acetic anhydride; acetic acid; acetonitrile; 1: Bromination / 2: Metallation / 3: Substitution / 4: Acetylation / 5: Nitration / 6: Catalytic hydrogenation;
DOI:10.1016/S0040-4039(99)02257-1

Reference yield:

: 74866-17-4
3,4-dimethoxy-2-methyl-1-bromobenzene

: 264607-06-9
Acetic acid (R)-2-(6-amino-3,4-dimethoxy-2-methyl-phenyl)-1-methyl-ethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 80 percent / n-BuLi / tetrahydrofuran / -78 °C

2: tetrahydrofuran / -78 - 25 °C

3: 100 percent / Et₃N; DMAP / CH₂Cl₂ / 20 h / 25 °C

4: 87 percent / HNO₃ / acetic anhydride; acetic acid / 4 h / 0 °C

5: 86 percent / H₂ / Pd/C / methanol / 25 °C

With dmap; n-butyllithium; hydrogen; nitric acid; triethylamine; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; acetic anhydride; acetic acid; 1: Metallation / 2: Substitution / 3: Acetylation / 4: Nitration / 5: Catalytic hydrogenation;
DOI:10.1016/S0040-4039(99)02257-1