[2-(2,2-Bis-phenylsulfanyl-ethyl)-4-oxo-azetidin-1-yl]-oxo-acetic acid methyl ester

Base Information

• Chemical Name: [2-(2,2-Bis-phenylsulfanyl-ethyl)-4-oxo-azetidin-1-yl]-oxo-acetic acid methyl ester
• CAS No.: 116108-47-5
• Molecular Formula: C₂₀H₁₉NO₄S₂
• Molecular Weight: 401.507
• Mol file: 116108-47-5.mol

Synonyms:[2-(2,2-Bis-phenylsulfanyl-ethyl)-4-oxo-azetidin-1-yl]-oxo-acetic acid methyl ester

Chemical Property of [2-(2,2-Bis-phenylsulfanyl-ethyl)-4-oxo-azetidin-1-yl]-oxo-acetic acid methyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of [2-(2,2-Bis-phenylsulfanyl-ethyl)-4-oxo-azetidin-1-yl]-oxo-acetic acid methyl ester

There total 4 articles about [2-(2,2-Bis-phenylsulfanyl-ethyl)-4-oxo-azetidin-1-yl]-oxo-acetic acid methyl 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: 100.0%

monomethyl oxalyl chloride (5781-53-3) + 4-(2,2-Bis-phenylsulfanyl-ethyl)-azetidin-2-one (116108-45-3) → [2-(2,2-Bis-phenylsulfanyl-ethyl)-4-oxo-azetidin-1-yl]-oxo-acetic acid methyl ester (116108-47-5)

Guidance literature:

With triethylamine; In dichloromethane; at -25 - -10 ℃; for 0.25h;

DOI:10.1039/c39880000544

Reference yield:

(4RS)-1-(tert-butyl-dimethylsilyl)-4-(2-oxoethyl)-2-oxoazetidine (67501-93-3) → [2-(2,2-Bis-phenylsulfanyl-ethyl)-4-oxo-azetidin-1-yl]-oxo-acetic acid methyl ester (116108-47-5)

Guidance literature:

Multi-step reaction with 2 steps

1: BF₃*OEt₂ / acetonitrile / 1 h / 0 °C

2: 100 percent / Et₃N / CH₂Cl₂ / 0.25 h / -25 - -10 °C

With boron trifluoride diethyl etherate; triethylamine; In dichloromethane; acetonitrile;

DOI:10.1039/c39880000544

Reference yield:

thiophenol (108-98-5) → [2-(2,2-Bis-phenylsulfanyl-ethyl)-4-oxo-azetidin-1-yl]-oxo-acetic acid methyl ester (116108-47-5)

Guidance literature:

Multi-step reaction with 2 steps

1: BF₃*OEt₂ / acetonitrile / 1 h / 0 °C

2: 100 percent / Et₃N / CH₂Cl₂ / 0.25 h / -25 - -10 °C

With boron trifluoride diethyl etherate; triethylamine; In dichloromethane; acetonitrile;

DOI:10.1039/c39880000544

upstream raw materials:

monomethyl oxalyl chloride

4-(2,2-Bis-phenylsulfanyl-ethyl)-azetidin-2-one

(4RS)-1-(tert-butyl-dimethylsilyl)-4-(2-oxoethyl)-2-oxoazetidine

thiophenol

Downstream raw materials:

methyl 1-carbapen-2-em-3-carboxylate