HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 68132626, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | HCID 68132302 | HCID 68132302 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 68132626 | HCID 68132626 | — |
Reaction Steps
The free base isolated from 8.0 g. of rac.-4-(3-chlorophenyl)-1,2,3,4-tetrahydro-7-methoxyisoquinoline hydrochloride is taken up in 150 ml. of methanol, 6 ml. of a 35% formaldehyde solution are added and the mixture is shaken until the precipitate formed again completely dissolves. The mixture is thereupon hydrogenated over 6 g. of Raney nickel, filtered and, after acidification with ethanolic hydrogen chloride, crystallized. Recrystallization from methanol-ether gives rac.-4-(3-chlorophenyl)-1,2,3,4-tetrahydro-7-methoxy-2-methylisoquinoline hydrochloride, m.p. 250°-251°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03947456 |
| Source dataset | uspto-grants-1976_03 |
| ORD ID | ord-530305ceee884556af78ad6481a756e0 |
| Source note | uspto-grants-1976_03 |