HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 3-Phenyl-3H-spiro[2-benzofuran-1,4'-piperidine]
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 86733482 | HCID 86733482 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Phenyl-3H-spiro[2-benzofuran-1,4'-piperidine] | HCID 191510 | — |
Reaction Steps
A mixture of 2.9 G. of 1'-benzyl-1,3-dihydro-3-phenylspiro[phenylspiro[isobenzofuran-1,4'-piperidine], (Example 4), 0.4 g. of 10% palladium on carbon, 20 ml. of 95% ethanol, and 2 ml. of conc. hydrochloric acid is hydrogenated at 50 p.s.i. and 50°. After hydrogen uptake ceases, the mixture is filtered and the filtrate concentrated. Recrystallization of the residue from cyclohexane provides colorless crystals, m.p. 119°-123°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03959475 |
| Source dataset | uspto-grants-1976_05 |
| ORD ID | ord-9c2f915bdfe7497d8e74b2e39d611e7b |
| Source note | uspto-grants-1976_05 |