The three-dimensional configuration of the ester heterocycle is basically the same as that of the carbocycle. Compound: 1-(Furan-2-yl)propan-1-one(SMILESS: O=C(C1=CC=CO1)CC,cas:3194-15-8) is researched.Reference of (R)-Piperidin-3-ol hydrochloride. The article 《Hydrothermal formation of hydroxylated benzenes from furan derivatives》 in relation to this compound, is published in Journal of Analytical and Applied Pyrolysis. Let’s take a look at the latest research on this compound (cas:3194-15-8).
Several furan derivatives were subjected to hydrothermolysis at 340° and 27.5 MPa for 1-33 min in a flow system to study their conversion to hydroxylated benzenes. Hydrothermolysis of 0.05M aqueous 5-methyl-2-furaldehyde, 2-acetylfuran and 2-propionylfuran gave 1,4-benzenediol, 1,2-benzenediol and 3-methyl-1,2-benzenediol, resp., with selectivities ranging from 10-65%. Hydrothermolysis of 0.01M aqueous 2-acetyl-5-(hydroxymethyl)furan and 5-(1-hydroxyethyl)-2-furaldehyde did not produce the expected benzenetriols; instead, 2-methyl-1,4-benzenediol could be identified as a product. Hydrothermolysis of 2-vinylfuran did not produce any phenol, an indication that the formation of benzene rings from furans is not accomplished by electrocyclic ring closure. 2,6-Dimethyl-γ-pyrone, a compound that is known to produce 5-methyl-1,3-benzenediol via an aldol condensation under alk. conditions, also gave this product under hydrothermal conditions. A reaction pathway for the hydrothermal formation of hydroxylated benzenes from furan derivatives is presented which is based on C ring formation via an intramol. aldol condensation.
There is still a lot of research devoted to this compound(SMILES:O=C(C1=CC=CO1)CC)Quality Control of 1-(Furan-2-yl)propan-1-one, and with the development of science, more effects of this compound(3194-15-8) can be discovered.
Reference:
Benzoxazole – Wikipedia,
Benzoxazole | C7H5NO – PubChem