Identification of Molecular Crystals Capable of Undergoing an Acyl‐Transfer Reaction Based on Intermolecular Interactions in the Crystal Lattice |
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Authors: | Majid I. Tamboli Dr. Shobhana Krishnaswamy Dr. Rajesh G. Gonnade Dr. Mysore S. Shashidhar |
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Affiliation: | 1. Division of Organic Chemistry, CSIR–National Chemical Laboratory, Dr. Homi Bhabha Road, Pashan, Pune‐411008 (India), Fax: (+91)?20‐25902629;2. Center for Materials Characterization, CSIR–National Chemical Laboratory, Dr. Homi Bhabha Road, Pashan, Pune‐411008 (India) |
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Abstract: | Investigation of the intermolecular acyl‐transfer reactivity in molecular crystals of myo‐inositol orthoester derivatives and its correlation with crystal structures enabled us to identify the essential parameters to support efficient acyl‐transfer reactions in crystals: 1) the favorable geometry of the nucleophile (? OH) and the electrophile (C?O) and 2) the molecular assembly, reinforced by C? H???π interactions, which supports a domino‐type reaction in crystals. These parameters were used to identify another reactive crystal through a data‐mining study of the Cambridge Structural Database. A 2:1 co‐crystal of 2,3‐naphthalene diol and its di‐p‐methylbenzoate was selected as a potentially reactive crystal and its reactivity was tested by heating the co‐crystals in the presence of solid sodium carbonate. A facile intermolecular p‐toluoyl group transfer was observed as predicted. The successful identification of reactive crystals opens up a new method for the detection of molecular crystals capable of exhibiting acyl‐transfer reactivity. |
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Keywords: | acylation domino reactions intermolecular interactions solid‐state reactions X‐ray diffraction |
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