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Home  > (S)-1-Benzyl-5-(((tert-butyldimethylsilyl)oxy)methyl)pyrrolidin-2-one

BL17307

109021-54-7 | (S)-1-Benzyl-5-(((tert-butyldimethylsilyl)oxy)methyl)pyrrolidin-2-one

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% 2 weeks $62.00 $44.00 -   +
250mg 95% 2 weeks $91.00 $64.00 -   +
1g 95% 2 weeks $127.00 $89.00 -   +
5g 95% 2 weeks $179.00 $125.00 -   +
25g 95% 2 weeks $848.00 $594.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: BL17307
Chemical Name: (S)-1-Benzyl-5-(((tert-butyldimethylsilyl)oxy)methyl)pyrrolidin-2-one
CAS Number: 109021-54-7
Molecular Formula: C18H29NO2Si
Molecular Weight: 319.5139
MDL Number: MFCD18071611
SMILES: O=C1CC[C@H](N1Cc1ccccc1)CO[Si](C(C)(C)C)(C)C

 

Upstream Synthesis Route
  • (S)-1-Benzyl-5-(((tert-butyldimethylsilyl)oxy)methyl)pyrrolidin-2-one is a versatile compound widely used in chemical synthesis as a key building block for the preparation of various complex organic molecules. Due to its unique structure, this compound serves as a valuable intermediate in the synthesis of pharmaceuticals, natural products, and other fine chemicals.In chemical synthesis, (S)-1-Benzyl-5-(((tert-butyldimethylsilyl)oxy)methyl)pyrrolidin-2-one can be utilized as a chiral auxiliary, enabling the introduction of chirality in target molecules. Its pyrrolidinone moiety facilitates selective functional group transformations, such as alkylations or acylations, leading to the formation of enantiomerically enriched compounds. Furthermore, the tert-butyldimethylsilyl (TBS) group can serve as a protecting group, safeguarding specific functional groups during synthetic manipulations.Additionally, the benzyl group provides stability and can be selectively removed under mild conditions, allowing for further elaboration of the molecule. The combination of these functionalities makes (S)-1-Benzyl-5-(((tert-butyldimethylsilyl)oxy)methyl)pyrrolidin-2-one a valuable tool in asymmetric synthesis, enabling chemists to access structurally diverse and stereochemically complex molecules efficiently and with high selectivity.
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