HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → 1-Piperidineacetic acid, ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Acetoxy-2-bromoethane | HCID 13564 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Piperidineacetic acid, ethyl ester | HCID 643466 | 89% |
Reaction Steps
To a solution of bromoethylacetate, 3.3 g (30.0 mmol) in 100 mL of tetrahydrofuran was added 4.2 mL (30.0 mmol) of Et3N and 9 mL (90.0 mmol) of piperidine. The reaction mixture stirred overnight at rt. and was concentrated to dryness. The residue was partitioned between chloroform and saturated aqueous NaHCO3. The mixture was washed with saturated NaHCO3, washed with brine, dried over Na2SO4, filtered and concentrated to dryness to give 4.6 g (89%) of the desired product as a tan oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06743794B2 |
| Source dataset | uspto-grants-2004_06 |
| ORD ID | ord-7989397a82ec49b1a43eb8297064ea67 |
| Source note | uspto-grants-2004_06 |