(2S,5R,6S)-Benzyl 3,3-Dimethyl-7-oxo-6-<<(trifluoromethyl)sulfonyl>oxy>-4-thia-1-azabicyclo<3.2.0>heptane-2-carboxylate

Base Information

Chemical Name:(2S,5R,6S)-Benzyl 3,3-Dimethyl-7-oxo-6-<<(trifluoromethyl)sulfonyl>oxy>-4-thia-1-azabicyclo<3.2.0>heptane-2-carboxylate
CAS No.:128971-96-0
Molecular Formula:C₁₆H₁₆F₃NO₆S₂
Molecular Weight:439.433
Hs Code.:

Synonyms:(2S,5R,6S)-Benzyl 3,3-Dimethyl-7-oxo-6-<<(trifluoromethyl)sulfonyl>oxy>-4-thia-1-azabicyclo<3.2.0>heptane-2-carboxylate

Suppliers and Price of (2S,5R,6S)-Benzyl 3,3-Dimethyl-7-oxo-6-<<(trifluoromethyl)sulfonyl>oxy>-4-thia-1-azabicyclo<3.2.0>heptane-2-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 (2S,5R,6S)-Benzyl 3,3-Dimethyl-7-oxo-6-<<(trifluoromethyl)sulfonyl>oxy>-4-thia-1-azabicyclo<3.2.0>heptane-2-carboxylate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (2S,5R,6S)-Benzyl 3,3-Dimethyl-7-oxo-6-<<(trifluoromethyl)sulfonyl>oxy>-4-thia-1-azabicyclo<3.2.0>heptane-2-carboxylate

There total 7 articles about (2S,5R,6S)-Benzyl 3,3-Dimethyl-7-oxo-6-<<(trifluoromethyl)sulfonyl>oxy>-4-thia-1-azabicyclo<3.2.0>heptane-2-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:

: 421-83-0
trifluoromethane sulfonyl chloride

: 51056-25-8
(2S,5R,6S)-Benzyl 6-Hydroxy-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo<3.2.0>heptane-2-carboxylate

: 128971-96-0
(2S,5R,6S)-Benzyl 3,3-Dimethyl-7-oxo-6-<<(trifluoromethyl)sulfonyl>oxy>-4-thia-1-azabicyclo<3.2.0>heptane-2-carboxylate

Guidance literature:: With triethylamine; In dichloromethane; at 0 ℃; for 0.25h;
DOI:10.1021/jo00304a024

Reference yield:

: 128971-90-4
(3S,4R)-3-<(tert-Butyldiphenylsilyl)oxy>-4-<(2-methyl-3-buten-2-yl)thio>-2-azetidinone

: 128971-96-0
(2S,5R,6S)-Benzyl 3,3-Dimethyl-7-oxo-6-<<(trifluoromethyl)sulfonyl>oxy>-4-thia-1-azabicyclo<3.2.0>heptane-2-carboxylate

Guidance literature:: Multi-step reaction with 7 steps

1: 90 percent / 2,6-lutidine / tetrahydrofuran / 2 h / -78 °C

2: 1) ozone, 2) Me₂S / 1) CH₂Cl₂, -78 deg C, 2) 0 deg C, 15 min

3: 1) t-BuOK / 1) THF, t-BuOH, 0 deg C, 15 min, 2) 0 deg C, 40 h

4: 62 percent / Et₃N, AcCl / CH₂Cl₂ / 20 h / 0 °C

5: 1) tetrabutylammonium fluoride, 2) ozone / 1) THF, -78 deg C, 1 h, 2) CH₂Cl₂, -78 deg C

6: 89 percent / DBU / CH₂Cl₂ / 8 h / Ambient temperature

7: 40 mg / Et₃N / CH₂Cl₂ / 0.25 h / 0 °C

With 2,6-dimethylpyridine; dimethylsulfide; potassium tert-butylate; tetrabutyl ammonium fluoride; ozone; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; acetyl chloride; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jo00304a024

Reference yield:

: 128971-92-6
(3S,4R)-3-<(tert-Butyldiphenylsilyl)oxy>-1-<(2,3-dimethyl-2-butyl)dimethylsilyl>-4-<(2-methyl-3-oxo-2-propyl)thio>-2-azetidinone

: 128971-96-0
(2S,5R,6S)-Benzyl 3,3-Dimethyl-7-oxo-6-<<(trifluoromethyl)sulfonyl>oxy>-4-thia-1-azabicyclo<3.2.0>heptane-2-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1: 1) t-BuOK / 1) THF, t-BuOH, 0 deg C, 15 min, 2) 0 deg C, 40 h

2: 62 percent / Et₃N, AcCl / CH₂Cl₂ / 20 h / 0 °C

3: 1) tetrabutylammonium fluoride, 2) ozone / 1) THF, -78 deg C, 1 h, 2) CH₂Cl₂, -78 deg C

4: 89 percent / DBU / CH₂Cl₂ / 8 h / Ambient temperature

5: 40 mg / Et₃N / CH₂Cl₂ / 0.25 h / 0 °C

With potassium tert-butylate; tetrabutyl ammonium fluoride; ozone; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; acetyl chloride; In dichloromethane;
DOI:10.1021/jo00304a024