HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-(5-Methyl-2-phenyl-4-oxazolylmethoxy) benzofuran-2-methanol → 6-(5-Methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofurancarbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-(5-Methyl-2-phenyl-4-oxazolylmethoxy) benzofuran-2-methanol | HCID 54094992 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-(5-Methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofurancarbaldehyde | HCID 19694372 | 69% |
Reaction Steps
A mixture of 6-(5-methyl-2-phenyl-4-oxazolylmethoxy) benzofuran-2-methanol (21.0 g), activated manganese dioxide (52.0 g) and tetrahydrofuran (800 ml) was stirred at 60° to 65° C. for 6 hours. After the insoluble portion was filtered off, the filtrate was concentrated; the residue was subjected to silica gel column chromatography. From the fraction eluted with ethyl acetate-chloroform (2:98, v/v), crystals of 6-(5-methyl-2-phenyl-4-oxazolylmethoxy) benzofuran-2-carbaldehyde (14.3 g, 69%) were obtained, which was then recrystallized from dichloromethane-isopropyl propyl ether to yield colorless prisms having a melting point of 137° to 138° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05723479 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-8d150316356a42dca5493597307eba01 |
| Source note | uspto-grants-1998_03 |