HuagongsheHuagongshe Chemistry Print Report · For research reference only
(4-Phenylsulfanylmethyl-phenyl)-methanol → 4-[(Phenylsulfanyl)methyl]benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (4-Phenylsulfanylmethyl-phenyl)-methanol | HCID 59255239 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 4-[(Phenylsulfanyl)methyl]benzaldehyde | HCID 820241 | 99.9% |
Reaction Steps
To a chloroform (10 mL) solution of (4-phenylsulfanylmethyl-phenyl)-methanol (1 g, 4.34 mmol) described in Manufacturing Example 206-1-2 was added manganese dioxide (3.77 g, 43.4 mmol), which was stirred for 15 hours at room temperature. The manganese dioxide was removed with a Celite bed, and the filtrate was concentrated under a reduced pressure to obtain the title compound (990 mg). The title compound was used in the following reaction without any further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08158657B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-8f6aea560b9d413ab1ebfb8f5cbd8ec0 |
| Source note | uspto-grants-2012_04 |