HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-(2-Hydroxy-ethyl)-4-(4-methyl-benzyl)-piperidin-4-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Bromoethanol | HCID 10898 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(4-Methylbenzyl)-piperidin-4-ol | HCID 10536242 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 1-(2-Hydroxy-ethyl)-4-(4-methyl-benzyl)-piperidin-4-ol | HCID 54242644 | 73% |
Reaction Steps
A mixture containing 4-(4-methyl-benzyl)-piperidin-4-ol (5.1 g, 25 mmol), 2-bromoethanol (1.8 ml, 25 mmol) and K2CO3 (5.2 g, 37.5 mmol) in 2-butanone (120 ml) was refluxed for 22 hours. H2O (30 ml) was added and the aqueous phase was extracted with ethylacetate. Combined organic phases were dried over Na2SO4, and concentrated. The residue was chromatographed over silica gel (CH2Cl2 --MeOH, 9:1 +NH4OH (1%)) to provide 1-(2-hydroxy-ethyl)-4-(4-methyl-benzyl)-piperidin-4-ol (4.3 g, 73%) as a yellow oil, MS: m/e=235.3 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05889026 |
| Source dataset | uspto-grants-1999_03 |
| ORD ID | ord-a8e9398e02fe4181bd2c8533d7b06be0 |
| Source note | uspto-grants-1999_03 |