RESUMO
The title compound, C(14)H(15)F(3)N(2)O(4)S·C(2)H(5)OH, was prepared by reaction of 4-hy-droxy-benzaldehyde, ethyl 4,4,4-trifluoro-3-oxobutano-ate and thio-urea. The hexa-hydro-pyrimidine ring adopts a half-chair conformation, the mean plane formed by the ring atoms excluding the C atom bonded to the eth-oxy-carbonyl group has an r.m.s. deviation of 0.0333â Å, and the dihedral angle between this plane and the benzene ring is 56.76â (5)°. The mol-ecular conformation is stabilized by an intra-molecular O-Hâ¯O hydrogen bond, generating an S(6) ring. The crystal structure is stabilized by inter-molecular O-Hâ¯O, O-Hâ¯S, N-Hâ¯O and N-Hâ¯S hydrogen bonds. The ethyl group of the ester unit is disordered over two positions, with an occupancy ratio of 0.757â (10):0.243â (10).