HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 15113388, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | HCID 13072903 | HCID 13072903 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 15113388 | HCID 15113388 | — |
Reaction Steps
(+)- 7 -methoxy- 4 -phenyl- 1,2,3,4 tetrahydroisoquinoline (2.4 g) was dissolved in methanol (50 ml) and 35% formaldehyde solution (3 ml) was added. The solution was stirred at ambient temperature for two hours when Raney nickel (1 g) was added and the solution hydrogenated at Atmospheric Pressure. The catalyst was removed by filtration, washed with ethanol and the filtrate and washings evaporated under reduced pressure to give the title compound as a colourless oil. Treatment of the title compound with ethereal hydrogen chloride gave its hydrochloride salt (2.3 g), m.p. 242° - 3° C. (dec) (methanol-ether) [α]D25 + 21.8° (water).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04113869 |
| Source dataset | uspto-grants-1978_09 |
| ORD ID | ord-6b7c50bc636545c0bb1f632aad502891 |
| Source note | uspto-grants-1978_09 |