HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4-Dihydro-6-methoxy-5-(phenylmethoxy)-2(1H)-isoquinolinecarboxaldehyde → HCID 21446991, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4-Dihydro-6-methoxy-5-(phenylmethoxy)-2(1H)-isoquinolinecarboxaldehyde | HCID 21447037 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 21446991 | HCID 21446991 | 92% |
Reaction Steps
89.2 g of 5-benzyloxy-2-formyl-1,2,3,4-tetrahydro-6-methoxy-isoquinoline are dissolved in 450 ml of glacial acetic acid and hydrogenated at room temperature and normal pressure in the presence of 4.5 g of 5 percent palladium black. After conclusion of hydrogen absorption, the reaction mixture is separated from the catalyst by filtration and evaporated to dryness under reduced pressure. Recrystallization of the residue from ethanol gives 57.2 g of 2-formyl-1,2,3,4-tetrahydro-5-hydroxy-6-methoxy-isoquinoline. m.p. = 172.5° - 173.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04013663 |
| Source dataset | uspto-grants-1977_03 |
| ORD ID | ord-0840521759c84c31aff50d2e2ba013ab |
| Source note | uspto-grants-1977_03 |