HuagongsheHuagongshe Chemistry Print Report · For research reference only
(5,6,7,8-Tetrahydroisoquinolin-3-yl)methanol → 5,6,7,8-Tetrahydroisoquinoline-3-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (5,6,7,8-Tetrahydroisoquinolin-3-yl)methanol | HCID 18799805 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5,6,7,8-Tetrahydroisoquinoline-3-carbaldehyde | HCID 18799578 | 77.1% |
Reaction Steps
A solution of 5,6,7,8-tetrahydro-3-isoquinolinylmethanol (572 mg, 3.50 mmol) in (DCM) (10 ml) at rt under argon was treated with manganese dioxide (3.047 g, 35.0 mmol) and then stirred at rt for 2 h. The reaction mixture was then filtered through a thin pad of Kieselguhr, eluting with DCM (50 ml), the organic extracts were evaporated to give the crude product as a brown oil (435 mg, 77%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08389524B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-b19c5a977e604a02bf151ce9f30ee29f |
| Source note | uspto-grants-2013_03 |