HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-t-Butyldimethylsilyloxymethyl-6-hydroxymethylnaphthalene → 2-t-Butyldimethylsilyloxylmethylnaphthalene-6-carboxaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-t-Butyldimethylsilyloxymethyl-6-hydroxymethylnaphthalene | HCID 23079298 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-t-Butyldimethylsilyloxylmethylnaphthalene-6-carboxaldehyde | HCID 23079328 | 96.7% |
Reaction Steps
The compound (255 mg) obtained in Example 121-2 was dissolved in chloroform (5.0 ml) and then added with manganese dioxide (chemically processed product) (366 mg), followed by stirring overnight at room temperature. After completion of the reaction, the solution was filtrated through Celite and the solvent was then distilled off, thereby obtaining the subject compound (245 mg) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07176227B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-3c8407cb9a60447980da25cca394a72f |
| Source note | uspto-grants-2007_02 |