3-<7-chloro-3-(S)-hydroxy-2-(R)-phenylheptanoyl>-4-(R)-phenyl-2-oxazolidinone

Base Information

• Chemical Name: 3-<7-chloro-3-(S)-hydroxy-2-(R)-phenylheptanoyl>-4-(R)-phenyl-2-oxazolidinone
• CAS No.: 220858-71-9
• Molecular Formula: C₂₂H₂₄ClNO₄
• Molecular Weight: 401.89
• Mol file: 220858-71-9.mol

Synonyms:3-<7-chloro-3-(S)-hydroxy-2-(R)-phenylheptanoyl>-4-(R)-phenyl-2-oxazolidinone

Chemical Property of 3-<7-chloro-3-(S)-hydroxy-2-(R)-phenylheptanoyl>-4-(R)-phenyl-2-oxazolidinone

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 3-<7-chloro-3-(S)-hydroxy-2-(R)-phenylheptanoyl>-4-(R)-phenyl-2-oxazolidinone

There total 3 articles about 3-<7-chloro-3-(S)-hydroxy-2-(R)-phenylheptanoyl>-4-(R)-phenyl-2-oxazolidinone 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:

phenylacetic acid (103-82-2) → 3-<7-chloro-3-(S)-hydroxy-2-(R)-phenylheptanoyl>-4-(R)-phenyl-2-oxazolidinone (220858-71-9)

Guidance literature:

Multi-step reaction with 2 steps

1: 78 percent / pivaloyl chloride, triethylamine / toluene

With pivaloyl chloride; triethylamine; In toluene;

DOI:10.1021/jo9821473

Reference yield:

(4R)-phenyl-2-oxazolidinone (90319-52-1,7480-32-2) → 3-<7-chloro-3-(S)-hydroxy-2-(R)-phenylheptanoyl>-4-(R)-phenyl-2-oxazolidinone (220858-71-9)

Guidance literature:

Multi-step reaction with 2 steps

1: 78 percent / pivaloyl chloride, triethylamine / toluene

With pivaloyl chloride; triethylamine; In toluene;

DOI:10.1021/jo9821473

Reference yield:

5-chloro-pentanal (20074-80-0) + (4R)-3-phenylacetyl-4-phenyl-1,3-oxazolidin-2-one (161745-73-9) → 3-<7-chloro-3-(S)-hydroxy-2-(R)-phenylheptanoyl>-4-(R)-phenyl-2-oxazolidinone (220858-71-9)

Guidance literature:

Yield given; Multistep reaction;

DOI:10.1021/jo9821473

upstream raw materials:

5-chloro-pentanal

(4R)-3-phenylacetyl-4-phenyl-1,3-oxazolidin-2-one

phenylacetic acid

(4R)-phenyl-2-oxazolidinone

Downstream raw materials:

3-<7-chloro-3-(S)-(methylsulfonyl)oxy-2-(R)-phenylheptanoyl>-4-(R)-phenyl-2-oxazolidinone

β-(R)-phenyl-1-(phenylmethyl)-2-(R)-piperidineethanol

(2R,3S)-7-Chloro-3-methanesulfonyloxy-2-phenyl-heptanoic acid methyl ester

α-(S)-(4-chlorobutyl)-β-(S)-(hydroxymethyl)benzeneethanol methanesulfonate