HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → [3,5-Bis(dimethylamino)-4-(piperidin-1-yl)phenyl]methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Methyl 3,5-bis(dimethylamino)-4-(piperidin-1-yl)benzoate | HCID 20290445 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | [3,5-Bis(dimethylamino)-4-(piperidin-1-yl)phenyl]methanol | HCID 53863713 | — |
Reaction Steps
A solution of 25 g. of methyl 3,5-bis(dimethylamino)-4-piperidinobenzoate in 150 ml. of absolute tetrahydrofuran was added dropwise to a solution of lithium aluminum hydride in 300 ml. of absolute tetrahydrofuran, and the mixture was boiled under reflux for 3 hours. After cooling, the excess lithium aluminum hydride was cautiously decomposed with 100 ml. of ethyl acetate and then with 3 ml. of water and the sodium evaporated to dryness. The residue was taken up in water, the oily product extracted with ethyl acetate and the ethyl acetate solution dried and evaporated. After recrystallization from high-boiling petroleum ether, there was obtained 3,5-bis(dimethylamino)-4-piperidinobenzyl alcohol having a melting point of 90°-92° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04039543 |
| Source dataset | uspto-grants-1977_08 |
| ORD ID | ord-0e5870098daf490c8e4cb65e6406183d |
| Source note | uspto-grants-1977_08 |