5-[(S)-2-((S)-4-Benzyl-2-oxo-oxazolidine-3-carbonyl)-butyl]-2-methoxy-benzoic acid

Base Information

• Chemical Name: 5-[(S)-2-((S)-4-Benzyl-2-oxo-oxazolidine-3-carbonyl)-butyl]-2-methoxy-benzoic acid
• CAS No.: 878268-34-9
• Molecular Formula: C₂₃H₂₅NO₆
• Molecular Weight: 411.455
• Mol file: 878268-34-9.mol

Synonyms:5-[(S)-2-((S)-4-Benzyl-2-oxo-oxazolidine-3-carbonyl)-butyl]-2-methoxy-benzoic acid

Chemical Property of 5-[(S)-2-((S)-4-Benzyl-2-oxo-oxazolidine-3-carbonyl)-butyl]-2-methoxy-benzoic acid

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 5-[(S)-2-((S)-4-Benzyl-2-oxo-oxazolidine-3-carbonyl)-butyl]-2-methoxy-benzoic acid

There total 3 articles about 5-[(S)-2-((S)-4-Benzyl-2-oxo-oxazolidine-3-carbonyl)-butyl]-2-methoxy-benzoic acid 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:

5-[(S)-2-((S)-4-Benzyl-2-oxo-oxazolidine-3-carbonyl)-butyl]-2-methoxy-benzoic acid benzyl ester → 5-[(S)-2-((S)-4-Benzyl-2-oxo-oxazolidine-3-carbonyl)-butyl]-2-methoxy-benzoic acid (878268-34-9)

Guidance literature:

With hydrogen; palladium on activated charcoal; In ethyl acetate; at 20 ℃;

DOI:10.1016/j.bmcl.2005.10.049

Reference yield:

(S)-4-benzyl-3-butyryloxazolidin-2-one (111292-87-6,143097-11-4,112459-79-7) → 5-[(S)-2-((S)-4-Benzyl-2-oxo-oxazolidine-3-carbonyl)-butyl]-2-methoxy-benzoic acid (878268-34-9)

Guidance literature:

Multi-step reaction with 2 steps

1: LiHMDS / tetrahydrofuran / -40 - 20 °C

2: H₂ / Pd/C / ethyl acetate / 20 °C

With hydrogen; lithium hexamethyldisilazane; palladium on activated charcoal; In tetrahydrofuran; ethyl acetate;

DOI:10.1016/j.bmcl.2005.10.049

Reference yield:

benzyl 5-bromomethyl-2-methoxybenzoate (311771-67-2) → 5-[(S)-2-((S)-4-Benzyl-2-oxo-oxazolidine-3-carbonyl)-butyl]-2-methoxy-benzoic acid (878268-34-9)

Guidance literature:

Multi-step reaction with 2 steps

1: LiHMDS / tetrahydrofuran / -40 - 20 °C

2: H₂ / Pd/C / ethyl acetate / 20 °C

With hydrogen; lithium hexamethyldisilazane; palladium on activated charcoal; In tetrahydrofuran; ethyl acetate;

DOI:10.1016/j.bmcl.2005.10.049

upstream raw materials:

(S)-4-benzyl-3-butyryloxazolidin-2-one

benzyl 5-bromomethyl-2-methoxybenzoate

Downstream raw materials:

(S)-2-{3-[(3-Fluoro-4-trifluoromethyl-benzoylamino)-methyl]-4-methoxy-benzyl}-butyric acid benzyl ester

(S)-2-{3-[(2-Fluoro-4-trifluoromethyl-benzoylamino)-methyl]-4-methoxy-benzyl}-butyric acid benzyl ester

(S)-4-Benzyl-3-{(S)-2-[3-(tert-butyl-dimethyl-silanyloxymethyl)-4-methoxy-benzyl]-butyryl}-oxazolidin-2-one

(S)-2-[3-(1,3-Dioxo-1,3-dihydro-isoindol-2-ylmethyl)-4-methoxy-benzyl]-butyric acid benzyl ester