HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl bromoacetate → [4-(3-Methoxy-phenyl)-piperidin-1-yl]-acetic Acid Methyl Ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl bromoacetate | HCID 60984 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-(3-Methoxyphenyl)piperidine | HCID 10702890 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | [4-(3-Methoxy-phenyl)-piperidin-1-yl]-acetic Acid Methyl Ester | HCID 69252936 | 91% |
Reaction Steps
A mixture of 4-(3-Methoxy-phenyl)-piperidine (0.8 g, 4.2 mmol), methylbromoacetate (1.28 g, 8.38 mmol), diisopropylethylamine (3.7 mL, 21 mmol) and MeOH (40 mL) was refluxed for 3 h. The reaction mixture was concentrated in vacuo, and the residue was partitioned between water and EtOAc and extracted. The organic layer was washed with water, brine, dried and concentrated in vacuo to give the title compound as an oil (1.0 g, 91% yield). MS(ESI) 264.2 (M+H+)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07365085B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-1ae15fdc37d54ce7b0490ad22c5ef0c8 |
| Source note | uspto-grants-2008_04 |