HuagongsheHuagongshe Chemistry Print Report · For research reference only
(4-{[(2-Phenylethyl)(4-phenyl-1,3-thiazol-2-yl)amino]methyl}phenyl)methanol → 4-{[(2-Phenylethyl)(4-phenyl-1,3-thiazol-2-yl)amino]methyl}benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (4-{[(2-Phenylethyl)(4-phenyl-1,3-thiazol-2-yl)amino]methyl}phenyl)methanol | HCID 23111783 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-{[(2-Phenylethyl)(4-phenyl-1,3-thiazol-2-yl)amino]methyl}benzaldehyde | HCID 23157348 | 68% |
Reaction Steps
To a solution of (4-{[(2-phenylethyl)(4-phenyl-1,3-thiazol-2-yl)amino]methyl}phenyl)methanol (3.0 g, 7.49 mmol) in tetrahydrofuran (50 mL) was added manganese dioxide (1.95 g, 22.5 mmol), and the mixture was stirred at room temperature for 3 hr. The insoluble material was filtered off and the filtrate was concentrated. The residue was purified by silica gel column chromatography (5%-50% ethyl acetate/hexane) to give the title compound (2.02 g, yield 68%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07786165B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-9420b480468d4b9caf4dac459ecbeef8 |
| Source note | uspto-grants-2010_08 |