1-[(4S)-4-Benzyl-1,3-oxazolidin-2-one-3-yl]propyltriphenylphosphonium Tetrafluoroborate

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.

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Publication Details

Journal
Molbank
Published
2026-08-17
DOI
https://doi.org/10.3390/m2220
Primary Topic
Organophosphorus compounds synthesis
Type
article
Field-Weighted Citation Impact
0.00

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article

1-[(4S)-4-Benzyl-1,3-oxazolidin-2-one-3-yl]propyltriphenylphosphonium Tetrafluoroborate

Jakub Adámek, Agnieszka Październiok-Holewa, Natalia Sępek
Molbank
Organophosphorus compounds synthesis
article

1-[(4S)-4-Benzyl-1,3-oxazolidin-2-one-3-yl]propyltriphenylphosphonium Tetrafluoroborate

Jakub Adámek, Agnieszka Październiok-Holewa, Natalia Sępek
article en

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.

MolbankVol. 2026(4)
Silesian University of Technology (PL)
Silesian University of Technology
Clean water and sanitation
Openalex Percentile: Top 18%
Organophosphorus compounds synthesis
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