The discovery of graphene stimulated an intensive search for its analogs and derivatives. One of the most interesting derivatives is hydrographene called graphane. Calculations indicate that bulk graphane is thermodynamically more favorable than all CH hydrocarbons including benzene. At the same time, pressureinduced polymerization of hydrocarbons and their derivatives at room temperature leads to the formation of amorphous products or poorly ordered one-dimensional products such as polyacetylene and benzene-derived carbon nanothreads.Here, we report a high-pressure high-temperature synthesis of several millimetersized samples of bulk graphanes with the composition C-H(D) from benzene and graphene-derivative C-H-N 0.2 from pyridine. X-ray diffraction, transmission electron microscopy, and infrared spectroscopy of new materials reveal relatively large (several nanometers in size) crystalline grains of an sp 3 -bonded graphane lattice (3-cycle-4step, the orthorhombic structure with P bca space-group and parameters a = 9.5-9.8Å, b = 8.9-9.1Å, c = 17.1-17.3Å). The main hydrogen groups in samples are C-H groups connected by aliphatic bonds. The synthesized graphanes at atmospheric pressure are stable up to 500 • C. The macroscopic density of CH samples is 1.5-1.57 g cm −3 and the refractive index is 1.78-1.80. The absorption spectra of samples with a high degree of crystallization exhibits a weak absorption maximum at 2.8 eV, which is responsible for the yellow-orange color, large absorption maximum at 4 eV and an absorption edge associated with the width of the optical gap at 5.2 eV. The bulk modulus (30-37 GPa) and shear modulus (15-18 GPa) of the fabricated samples, as well as their hardness (1-1.5 GPa), are about twice as high as the respective values for polycrystalline graphite. The solution of metalorganic complexes in benzene and pyridine makes it possible to obtain doped graphanes, which can have extraordinary electron transport and magnetic properties.arXiv:1608.07221v1 [cond-mat.mtrl-sci]