HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → 1-Piperidineacetic acid, ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 1-Piperidineacetic acid, ethyl ester | HCID 643466 | 64% |
Reaction Steps
Ethyl bromoacetate (8.5 g, 50.9 mmol) was added dropwise to a stirred solution of piperidine (4.3 g, 50.5 mmol) and triethylamine (5.5 g, 54.4 mmol) in chloroform (20 ml) at such a rate as to maintain a gentle reflux. After the addition was complete stirring was continued for 2 hours and the reaction mixture washed with water (20 m×3). The choroform layer was dried (MgSO4) filtered and the solvent evaporated to leave a yellow oil. This oil was passed through a short column of silica eluting with a CH2Cl2/Pet Ether 40:60 mixture (1:1). Removal of the solvent from the resulting solution gave the required product as a pale yellow oil (Yield 5.5 g,64%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08022211B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-5ae616a311ef4ee7aea0ae27339e498b |
| Source note | uspto-grants-2011_09 |