allyl (1R,5R,6S)-2-phenyl-6-<(1R)-1-<(tert-butyldimethylsilyl)oxy>ethyl>-1-methylcarbapen-2-em-3-carboxylate

Base Information

Chemical Name:allyl (1R,5R,6S)-2-phenyl-6-<(1R)-1-<(tert-butyldimethylsilyl)oxy>ethyl>-1-methylcarbapen-2-em-3-carboxylate
CAS No.:107515-14-0
Molecular Formula:C₂₅H₃₅NO₄Si
Molecular Weight:441.643
Hs Code.:

Synonyms:allyl (1R,5R,6S)-2-phenyl-6-<(1R)-1-<(tert-butyldimethylsilyl)oxy>ethyl>-1-methylcarbapen-2-em-3-carboxylate

Suppliers and Price of allyl (1R,5R,6S)-2-phenyl-6-<(1R)-1-<(tert-butyldimethylsilyl)oxy>ethyl>-1-methylcarbapen-2-em-3-carboxylate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of allyl (1R,5R,6S)-2-phenyl-6-<(1R)-1-<(tert-butyldimethylsilyl)oxy>ethyl>-1-methylcarbapen-2-em-3-carboxylate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of allyl (1R,5R,6S)-2-phenyl-6-<(1R)-1-<(tert-butyldimethylsilyl)oxy>ethyl>-1-methylcarbapen-2-em-3-carboxylate

There total 9 articles about allyl (1R,5R,6S)-2-phenyl-6-<(1R)-1-<(tert-butyldimethylsilyl)oxy>ethyl>-1-methylcarbapen-2-em-3-carboxylate 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: 58.0%

: 107515-01-5
(3S,4R)-1-<<(allyloxy)carbonyl>(triphenylphosphoranylidene)methyl>-3-<(1R)-1-<(tert-butyldimethylsilyl)oxy>ethyl>-4-<(1R)-1-(phenylcarbonyl)ethyl>azetidin-2-one

: 107515-14-0
allyl (1R,5R,6S)-2-phenyl-6-<(1R)-1-<(tert-butyldimethylsilyl)oxy>ethyl>-1-methylcarbapen-2-em-3-carboxylate

Guidance literature:: In xylene; at 130 ℃; for 15h;
DOI:10.1021/jm00388a022

Reference yield:

: 57833-54-2,61879-31-0,107596-43-0
diallyl tartarate

: 107515-14-0
allyl (1R,5R,6S)-2-phenyl-6-<(1R)-1-<(tert-butyldimethylsilyl)oxy>ethyl>-1-methylcarbapen-2-em-3-carboxylate

Guidance literature:: Multi-step reaction with 7 steps

1: periodic acid / tetrahydrofuran / 1 h

2: toluene / 12 h / Heating

3: 6.2 g / thionyl chloride, pyridine / tetrahydrofuran / 0.75 h / -40 - -20 °C

4: 13.9 g / dimethylformamide / 1.5 h / Ambient temperature

5: triethylamine / CH₂Cl₂ / 1 h / 0 °C

6: 67 percent / tetrahydrofuran / 0.5 h / 0 °C

7: 58 percent / xylene / 15 h / 130 °C

With pyridine; thionyl chloride; periodic acid; triethylamine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; toluene; xylene;
DOI:10.1021/jm00388a022

Reference yield:

: 93711-85-4,97101-07-0,113033-46-8,120710-59-0,120710-60-3,90776-58-2
(2R)-2-[(2S,3S)-3-{(1R)-1-(t-butyldimethylsilyloxy)ethyl}-4-oxoazetidin-2-yl]propionic acid

: 107515-14-0
allyl (1R,5R,6S)-2-phenyl-6-<(1R)-1-<(tert-butyldimethylsilyl)oxy>ethyl>-1-methylcarbapen-2-em-3-carboxylate

Guidance literature:: Multi-step reaction with 7 steps

1: 73 percent / imidazole / dimethylformamide / 4 h / 47 °C

2: toluene / 12 h / Heating

3: 6.2 g / thionyl chloride, pyridine / tetrahydrofuran / 0.75 h / -40 - -20 °C

4: 13.9 g / dimethylformamide / 1.5 h / Ambient temperature

5: triethylamine / CH₂Cl₂ / 1 h / 0 °C

6: 67 percent / tetrahydrofuran / 0.5 h / 0 °C

7: 58 percent / xylene / 15 h / 130 °C

With pyridine; 1H-imidazole; thionyl chloride; triethylamine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; toluene; xylene;
DOI:10.1021/jm00388a022