Unexpected Formation of a Chiral <i>spiro</i> ‐system in the Reaction of the Dilithium Derivative of Hexafluorocumyl Alcohol with <i>N</i> ‐( <i>t–</i> butylsulfenyl)phthalimide

An unexpected course of the reaction of hexafluorocumyl alcohol dilithium derivative 2 with N-(t-butylsulfenyl)phthalimide (3) has been presented. The process proceeded under mild conditions and resulted in previously undescribed chiral spiro-system- 3',3'-bis(trifluoromethyl)-3H,3'H-1,1'-spirobis(isobenzofuran)-3-one (5) as the only product. A detailed spectral analysis of the product has been provided, and mechanistic aspects have been investigated. Attempts to separate the enantiomers of compound 5 using a semipreparative HPLC method with a chiral stationary phase column have been described. The repeatability of the reaction using analogs of alcohol 4 has also been tested. DFT calculations of absolute configuration assignment have been performed successfully.

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Publication Details

Journal
ChemPlusChem
Published
2024-11-26
DOI
https://doi.org/10.1002/cplu.202400614
Primary Topic
Analytical Chemistry and Chromatography
Type
article
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article

Unexpected Formation of a Chiral spiro ‐system in the Reaction of the Dilithium Derivative of Hexafluorocumyl Alcohol with N ‐( t– butylsulfenyl)phthalimide

A. Zając, Lesław Sieroń, J. Drabowicz, Remigiusz Żurawiński
ChemPlusChem
Analytical Chemistry and Chromatography
article

Unexpected Formation of a Chiral spiro ‐system in the Reaction of the Dilithium Derivative of Hexafluorocumyl Alcohol with N ‐( t– butylsulfenyl)phthalimide

A. Zając, Lesław Sieroń, J. Drabowicz, Remigiusz Żurawiński
article en

Abstract

An unexpected course of the reaction of hexafluorocumyl alcohol dilithium derivative 2 with N-(t-butylsulfenyl)phthalimide (3) has been presented. The process proceeded under mild conditions and resulted in previously undescribed chiral spiro-system- 3',3'-bis(trifluoromethyl)-3H,3'H-1,1'-spirobis(isobenzofuran)-3-one (5) as the only product. A detailed spectral analysis of the product has been provided, and mechanistic aspects have been investigated. Attempts to separate the enantiomers of compound 5 using a semipreparative HPLC method with a chiral stationary phase column have been described. The repeatability of the reaction using analogs of alcohol 4 has also been tested. DFT calculations of absolute configuration assignment have been performed successfully.

ChemPlusChemVol. 90(3)
Jan Długosz University (PL), Lodz University of Technology (PL), Science & Technology Park (Czechia) (CZ), Centrum Badań Molekularnych i Makromolekularnych Polskiej Akademii Nauk (PL), Adam Mickiewicz University in Poznań (PL), Polish Academy of Sciences (PL)
Clean water and sanitation
Openalex Percentile: Top 84%
Analytical Chemistry and Chromatography
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