HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-chloro-6-(piperidin-1-yl)-benzofuran-3(2H)-one → 5-Chloro-6-(piperidin-1-yl)-2,3-dihydrobenzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-chloro-6-(piperidin-1-yl)-benzofuran-3(2H)-one | HCID 20255664 | — |
| Catalyst | Platinum oxide (PtO) | HCID 82844 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Chloro-6-(piperidin-1-yl)-2,3-dihydrobenzofuran | HCID 20255636 | — |
Reaction Steps
200 mg of platinum oxide are added to a solution of 1.38 g (5.5 mmole) of 5-chloro-6-(piperidin-1-yl)-benzofuran-3(2H)-one in 20 ml of ethanol and the whole is hydrogenated at 3 atmospheres. The catalyst is filtered off and the filtrate is concentrated in a vacuum rotary evaporator. The residue is chromatographed over silica gel using methylene chloride as eluant. Recrystallisation from petroleum ether yields 5-chloro-6-(piperidin-1-yl)-2,3-dihydrobenzofuran having a melting point of 38°-40°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04558043 |
| Source dataset | uspto-grants-1985_12 |
| ORD ID | ord-1acbea09b980480ca2d8d59231e3c4db |
| Source note | uspto-grants-1985_12 |