This particular compound is synthesed starting from anthracene with a methyl group added to each arene ring (1,8,9-trimethylanthracene). A triptycene compound is formed from a reaction of this anthracene compound with an aryne in a Diels-Alder reaction in isoamyl nitrite. In this synthesis the precursor to the reactive aryne is 2-amino-6-methylbenzoic acid. Next the methyl substituents are functionalized with bromine groups by the photochemical reaction with N-bromosuccinimide or NBS. The final cyclophane is put together by reaction with 1,3,5-tris(mercaptomethyl)benzene with nucleophilic sulfhydryl groups and electrophilic alkyl bromides in a Nucleophilic aliphatic Substitution.
X-ray crystallography of the tri-sulfone derivative of this cyclophane shows that the methyl group located 2.896 angstroms (289.6 picometers) from the center of the benzene ring. The carbon to carbon bond linking the methyl group to the triptycene frame is actually shortened and measures 1.475 to 1.495 angstroms (147.5 to 149.5 pm). The similar bond in the triptycene precursor is 1.54 angstroms (154 pm). Proton NMR analysis shows a chemical shift of 2.52 ppm for the methyl protons compared to that of 3.16 to 3.85 in the anthracene compound. The reason for this anomaly is that the methyl protons are in line with the Aromatic ring current of the benzene ring and are therefore severely shielded. In certain paracyclophanes bridging methylene protons can even experience negative chemical shifts in proton NMR.