HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2110902Generated: October 27, 2026
Dimethylformamide → Methyl 3-[4-({4-[(4-hydroxypiperidin-1-yl)methyl]benzyl}oxy)phenyl]propanoate
https://huagongshe.com/reaction/2110902
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Piperidin-4-ol | HCID 79341 | — |
| Reactant | Methyl 3-(4-([4-(chloromethyl)benzyl]oxy)phenyl)propanoate | HCID 23082857 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 3-[4-({4-[(4-hydroxypiperidin-1-yl)methyl]benzyl}oxy)phenyl]propanoate | HCID 23159986 | 99.9% |
Reaction Steps
A mixture of methyl 3-(4-{[4-(chloromethyl)benzyl]oxy}phenyl)propanoate (0.6 g, 1.88 mmol), 4-hydroxypiperidine (0.29 g, 2.82 mmol), potassium carbonate (0.39 g, 2.82 mmol) and N,N-dimethylformamide (12 mL) was stirred at 60° C. for 21 hr. The reaction mixture was diluted with ethyl acetate, and the mixture washed with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to give the title compound (0.72 g, yield 99%) as a beige powder. MS (ESI+): 384 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07517910B2 |
|---|
| Source dataset | uspto-grants-2009_04 |
|---|
| ORD ID | ord-74d86cbe99464fb29f8c016a18749283 |
|---|
| Source note | uspto-grants-2009_04 |
|---|