Abstract
1-[(4S)-4-benzyl-1,3-oxazolidin-2-one-3-yl]propyltriphenylphosphonium tetrafluoroborate was synthesized in a two-step procedure starting from (4S)-4-benzyl-3-propionyl-1,3-oxazolidin-2-one. In the first step, (4S)-4-benzyl-3-propionyl-1,3-oxazolidin-2-one was treated with DIBAL-H at −78 °C in DCM and then converted to (4S)-4-benzyl-3-(1-trimethylsilyloxy)propyl-1,3-oxazolidin-2-one with TMSOTf at −78 °C in DCM in the presence of pyridine. Next, the silylated intermediate was transformed to the expected 1-[(4S)-4-benzyl-1,3-oxazolidin-2-one-3-yl]propyltriphenylphosphonium tetrafluoroborate by reaction with Ph3P·HBF4 at −40 °C in DCM. The structures of the compounds obtained were confirmed by spectroscopic methods (1H-, 13C{1H}-, 31P{1H}-NMR, IR) and HRMS analysis.
| Original language | Danish |
|---|---|
| Article number | M2220 |
| Journal | MolBank |
| Volume | 2026 |
| Issue number | 4 |
| DOIs | |
| Publication status | Published - Aug 2026 |
Keywords
- building blocks
- chiral auxiliary
- triphenylphosphonium salts
- α-amidoalkylating agents
- α-amidoalkylation
ASJC Scopus subject areas
- Biochemistry
- Physical and Theoretical Chemistry
- Organic Chemistry
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