HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 4-(Acetyloxy)-1-benzylpiperidine-4-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | 1-Benzyl-4-hydroxypiperidine-4-carboxylic acid hydrochloride | HCID 91844426 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(Acetyloxy)-1-benzylpiperidine-4-carboxylic acid | HCID 53302252 | 52% |
Reaction Steps
A mixture of 9.4 g 1-benzyl-4-hydroxy-piperidine-4-carboxylic acid, hydrochloride, 3.62 g (35 mmol) acetic anhydride, 11.89 mL pyridine in 40 mL DCM was stirred for 1 h at room temperature. KHSO4 (10%) and ethanol were added and filtered. The filtrate was evaporated and the residue was purified by preparative HPLC on reversed phase eluting with a gradient formed from acetonitrile, water and HCOOH. The product containing fractions were evaporated to yield 4.2 g (52%) of the title compound as light yellow solid. MS (m/e): 278.1 [(M+H)+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08399676B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-05f35b198e5c4219b434056fd391e32f |
| Source note | uspto-grants-2013_03 |