(-)-(4R)-4-(phenyldifluoromethyl)-3-propionyl-oxazolidin-2-one

Base Information

• Chemical Name: (-)-(4R)-4-(phenyldifluoromethyl)-3-propionyl-oxazolidin-2-one
• CAS No.: 1020850-60-5
• Molecular Formula: C₁₃H₁₃F₂NO₃
• Molecular Weight: 269.248
• Mol file: 1020850-60-5.mol

Synonyms:(-)-(4R)-4-(phenyldifluoromethyl)-3-propionyl-oxazolidin-2-one

Chemical Property of (-)-(4R)-4-(phenyldifluoromethyl)-3-propionyl-oxazolidin-2-one

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (-)-(4R)-4-(phenyldifluoromethyl)-3-propionyl-oxazolidin-2-one

There total 7 articles about (-)-(4R)-4-(phenyldifluoromethyl)-3-propionyl-oxazolidin-2-one 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: 87.0%

(-)-(4R)-4-(phenyldifluoromethyl)-oxazolidin-2-one (1020850-59-2) + propionyl chloride (79-03-8) → (-)-(4R)-4-(phenyldifluoromethyl)-3-propionyl-oxazolidin-2-one (1020850-60-5)

Guidance literature:

(-)-(4R)-4-(phenyldifluoromethyl)-oxazolidin-2-one; With sodium hydride; In N,N-dimethyl-formamide; at 0 ℃; for 0.333333h;

propionyl chloride; In N,N-dimethyl-formamide; at 0 ℃; for 1h; Further stages.;

DOI:10.1016/j.jfluchem.2007.03.001

Reference yield:

(-)-(2S,Ss)-3,3-difluoro-3-phenyl-2-[N-(p-methoxyphenyl)]aminopropyl-(1-naphthyl)sulfoxide (1020850-63-8) → (-)-(4R)-4-(phenyldifluoromethyl)-3-propionyl-oxazolidin-2-one (1020850-60-5)

Guidance literature:

Multi-step reaction with 5 steps

1.1: 78 percent / CAN; H₂O / acetonitrile / 20 °C

2.1: 92 percent / aq. K₂CO₃ / dioxane / 20 °C

3.1: TFAA; sym-collidine / acetonitrile / 0 °C

3.2: aq. K₂CO₃

3.3: 79 percent / NaBH₄ / H₂O

4.1: 91 percent / NaH / dimethylformamide / 0.5 h / 0 °C

5.1: NaH / dimethylformamide / 0.33 h / 0 °C

5.2: 87 percent / dimethylformamide / 1 h / 0 °C

With 2,4,6-trimethyl-pyridine; ammonium cerium(IV) nitrate; water; sodium hydride; potassium carbonate; trifluoroacetic anhydride; In 1,4-dioxane; N,N-dimethyl-formamide; acetonitrile; 3.1: Pummerer reaction;

DOI:10.1016/j.jfluchem.2007.03.001

Reference yield:

(+)-(Ss)-{3,3-difluoro-3-phenyl-2-[N-(p-methoxyphenyl)imino]propyl}-(1-naphthyl)sulfoxide (1020850-62-7) → (-)-(4R)-4-(phenyldifluoromethyl)-3-propionyl-oxazolidin-2-one (1020850-60-5)

Guidance literature:

Multi-step reaction with 6 steps

1.1: 91 percent / NaBH₄ / tetrahydrofuran; methanol / 5 h / -20 °C

2.1: 78 percent / CAN; H₂O / acetonitrile / 20 °C

3.1: 92 percent / aq. K₂CO₃ / dioxane / 20 °C

4.1: TFAA; sym-collidine / acetonitrile / 0 °C

4.2: aq. K₂CO₃

4.3: 79 percent / NaBH₄ / H₂O

5.1: 91 percent / NaH / dimethylformamide / 0.5 h / 0 °C

6.1: NaH / dimethylformamide / 0.33 h / 0 °C

6.2: 87 percent / dimethylformamide / 1 h / 0 °C

With 2,4,6-trimethyl-pyridine; sodium tetrahydroborate; ammonium cerium(IV) nitrate; water; sodium hydride; potassium carbonate; trifluoroacetic anhydride; In tetrahydrofuran; 1,4-dioxane; methanol; N,N-dimethyl-formamide; acetonitrile; 4.1: Pummerer reaction;

DOI:10.1016/j.jfluchem.2007.03.001

upstream raw materials:

(-)-(4R)-4-(phenyldifluoromethyl)-oxazolidin-2-one

propionyl chloride

(+)-(S_s)-{3,3-difluoro-3-phenyl-2-[N-(p-methoxyphenyl)imino]propyl}-(1-naphthyl)sulfoxide

(-)-(2S,S_s)-3,3-difluoro-3-phenyl-2-[N-(p-methoxyphenyl)]aminopropyl-(1-naphthyl)sulfoxide

Downstream raw materials:

(4R)-4-(phenyldifluoromethyl)-N-(2S,3R)-(3-hydroxy-2,4-dimethyl-pentanoyl)-1,3-oxazolidin-2-one

(4R)-4-(phenyldifluoromethyl)-N-(2R,3S)-(3-hydroxy-2,4-dimethyl-pentanoyl)-1,3-oxazolidin-2-one

(-)-(4R)-4-(phenyldifluoromethyl)-oxazolidin-2-one