The solid state of comb copolymer-like systems obtained by blending poly(4-vinylpyridine) with pentadecylphenol was studied by a combination of techniques. Depending on the amount of pentadecylphenol, several regimes are present. For 0.5 less than or equal to x less than or equal to 1.0 (x is the ratio between the number of phenol and pyridine groups) the alkyl tails form an interdigitated hexagonally packed crystalline layer. Small-angle X-ray scattering measurements show that for x 1.5 and 2.0 the excess pentadecylphenol cocrystallizes with the associated pentadecylphenol, with the free phenol groups probably aggregating near the middle of the crystalline layer. For x greater than or equal to 2.0 the orthorhombic crystal modification also appears. Finally for x greater than or equal to 3.0, part of the excess pentadecylphenol macrophase separates on crystallization, forming an additional phase of pure pentadecylphenol with the familiar orthorhombic packing. These findings are similar to results obtained for real comb copolymer systems, i.e., containing covalently bonded side chains. However, our systems are essentially different due to the dynamic hydrogen-bonding equilibrium, which implies that the equilibrium solid state may always involve some form of macrophase separation.