HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 12364533, compound → HCID 12364536, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 12364533 | HCID 12364533 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 12364536 | HCID 12364536 | 66.66% |
Reaction Steps
A solution of 1-benzyl-3-(2-oxo-2-phenylethyl)piperidin-4-one (4.0 g, 0.0129 mol) in conc. HCl (50 mL) was heated at reflux for 3 h. After consumption of the starting material as determined by TLC, the reaction mixture was cooled down to RT and made alkaline by the addition of NH4OH, then extracted with diethyl ether. The organics were dried over Na2SO4 and concentrated to afford 5-benzyl-2-phenyl-4,5,6,7-tetrahydrofuro[3,2-c]pyridine (2.0 g, 66.66%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09334269B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-fa44da748c9a40c9b8ec38c2965453e6 |
| Source note | uspto-grants-2016_05 |