(3R,4S)-1-benzoyl-3-<(tert-butyldimethylsilyl)oxy>-4-(2-pyridyl)-2-azetidinone

Base Information

Chemical Name:(3R,4S)-1-benzoyl-3-<(tert-butyldimethylsilyl)oxy>-4-(2-pyridyl)-2-azetidinone
CAS No.:158271-90-0
Molecular Formula:C₂₁H₂₆N₂O₃Si
Molecular Weight:382.535
Hs Code.:

Synonyms:(3R,4S)-1-benzoyl-3-<(tert-butyldimethylsilyl)oxy>-4-(2-pyridyl)-2-azetidinone

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

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Chemical Property of (3R,4S)-1-benzoyl-3-<(tert-butyldimethylsilyl)oxy>-4-(2-pyridyl)-2-azetidinone

Chemical Property:

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Technology Process of (3R,4S)-1-benzoyl-3-<(tert-butyldimethylsilyl)oxy>-4-(2-pyridyl)-2-azetidinone

There total 2 articles about (3R,4S)-1-benzoyl-3-<(tert-butyldimethylsilyl)oxy>-4-(2-pyridyl)-2-azetidinone 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:

: 1121-60-4
pyridine-2-carbaldehyde

: 158271-90-0
(3R,4S)-1-benzoyl-3-<(tert-butyldimethylsilyl)oxy>-4-(2-pyridyl)-2-azetidinone

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) n-BuLi / 1.) THF, 0 deg C, 0.5 h, 2.) -78 deg C, 0.5 h

2: 1.) LDA, 3.) Et₃N, DMAP / 1.) THF, -78 deg C, 2 h, 2.) -78 deg C, 3 h, 3.) CH₂Cl₂, 0 deg C, 15 min

With dmap; n-butyllithium; triethylamine; lithium diisopropyl amide;
DOI:10.1021/jo951961c

Reference yield:

: 98-88-4
benzoyl chloride

: 132127-26-5
2-O-<<(tert-butyldimethylsilyl)oxy>acetyl>-10-(dicyclohexylsulfamoyl)-D-isoborneol

: 135639-14-4
1,1,1-trimethyl-N-(pyridin-2-ylmethylene)silanamine

: 158271-90-0
(3R,4S)-1-benzoyl-3-<(tert-butyldimethylsilyl)oxy>-4-(2-pyridyl)-2-azetidinone

Guidance literature:: With dmap; triethylamine; lithium diisopropyl amide; Yield given. Multistep reaction; 1.) THF, -78 deg C, 2 h, 2.) -78 deg C, 3 h, 3.) CH₂Cl₂, 0 deg C, 15 min;
DOI:10.1021/jo951961c