organic compounds
Open access
In the title compound, C18H18O4, the six-membered chroman-4-one ring adopts an envelope conformation with the C atom bonded to the bridging CH2 atom as the flap. The dihedral angle between the mean plane of the fused pyranone ring and the dimethoxy-substituted benzene ring is 89.72 (2)°. In the crystal, adjacent molecules are linked via C—Hπ interactions.
organic compounds
Open access
In the title compound, C14H14BrNO5, the ester group is disordered [occupancy ratio 0.52 (2):0.48 (2)]. The major component is nearly coplanar with the benzofuran plane, subtending a dihedral angle of 7.84 (2)°, while the amide group is twisted out of the benzofuran plane making a dihedral angle of 39.69 (2)°. An intramolecular N—HO hydrogen bond occurs. In the crystal, pairs of weak C—HO hydrogen bonds link the molecules into inversion dimers, which are further linked via strong N—HO hydrogen bonds, generating a zigzag chain extending along [100].
organic compounds
Open access
The title compound, C11H10BrNO3, is close to planar with the benzofuran unit and the ester group subtending a dihedral angle of 5.25 (2)°. The molecular structure features an intramolecular N—HO interaction. In the crystal, N—HO hydrogen bonds involving carboxyl O-atom acceptors generate a chain extending along [201].
organic compounds
Open access
In the racemic title compound, C16H14O3, the ring of the 4-hydroxybenzyl substituent group forms a dihedral angle of 80.12 (12)° with the benzene ring of the chromanone system. Two C atoms of the pyranone ring and the H atoms on the benzyl α-C atom are disordered over two sites, with site-occupation factors of 0.818 (8) and 0.182 (8). The crystal structure is stabilized by O—HO hydrogen bonds, which form parallel one-dimensional zigzag chains down the c axis and are interconnected by both methine C—HO hydrogen bonds and weak aromatic C—Hπ interactions, giving a sheet structure lying parallel to [011].