4-(3,4-difluorophenyl)-2-oxo-oxazolidine-3-carboxylic acid-4-nitro-phenyl ester

Base Information

• Chemical Name: 4-(3,4-difluorophenyl)-2-oxo-oxazolidine-3-carboxylic acid-4-nitro-phenyl ester
• CAS No.: 218449-37-7
• Molecular Formula: C₁₆H₁₀F₂N₂O₆
• Molecular Weight: 364.262
• Mol file: 218449-37-7.mol

Synonyms:4-(3,4-difluorophenyl)-2-oxo-oxazolidine-3-carboxylic acid-4-nitro-phenyl ester

Chemical Property of 4-(3,4-difluorophenyl)-2-oxo-oxazolidine-3-carboxylic acid-4-nitro-phenyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 4-(3,4-difluorophenyl)-2-oxo-oxazolidine-3-carboxylic acid-4-nitro-phenyl ester

There total 8 articles about 4-(3,4-difluorophenyl)-2-oxo-oxazolidine-3-carboxylic acid-4-nitro-phenyl 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%

4-(3,4-difluorophenyl)-2-oxazolidinone (225641-91-8) + dichloromethane (75-09-2) + 4-Nitrophenyl chloroformate (7693-46-1) → 4-(3,4-difluorophenyl)-2-oxo-oxazolidine-3-carboxylic acid-4-nitro-phenyl ester (218449-37-7)

Guidance literature:

With NaH; In tetrahydrofuran; hexane;

Reference yield:

3,4 difluorobenzaldehyde (34036-07-2) → 4-(3,4-difluorophenyl)-2-oxo-oxazolidine-3-carboxylic acid-4-nitro-phenyl ester (218449-37-7)

Guidance literature:

Multi-step reaction with 5 steps

1: methanol; trimethylsilyl cyanide

2: sodium hydroxide; LiAlH₄ / water

3: chloroform; ethyl acetate

4: NaH / tetrahydrofuran; water

5: NaH / tetrahydrofuran; hexane

With sodium hydroxide; LiAlH₄; NaH; In tetrahydrofuran; methanol; hexane; chloroform; trimethylsilyl cyanide; water; ethyl acetate;

Reference yield:

2-amino-2-(3,4-difluorophenyl)-ethanol (277295-93-9,218449-32-2,1269935-50-3) → 4-(3,4-difluorophenyl)-2-oxo-oxazolidine-3-carboxylic acid-4-nitro-phenyl ester (218449-37-7)

Guidance literature:

Multi-step reaction with 3 steps

1: chloroform; ethyl acetate

2: NaH / tetrahydrofuran; water

3: NaH / tetrahydrofuran; hexane

With NaH; In tetrahydrofuran; hexane; chloroform; water; ethyl acetate;

upstream raw materials:

4-(3,4-difluorophenyl)-2-oxazolidinone

dichloromethane

4-Nitrophenyl chloroformate

2-amino-2-(3,4-difluorophenyl)-ethanol

Downstream raw materials:

(+)-3-(3-(4-cyano-4-(2,4-dichloro)phenylpiperidin-1-yl)propyl)aminocarbonyl-4-(3,4-difluorophenyl)-2-oxazolidinone

(+)-3-(3-(4-Aminocarbonyl-4-(4-chloro)phenylpiperidin-1-yl)-propyl)aminocarbonyl-4-(3,4-difluoro)phenyl-2-oxazolidinone