HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → [1-(Propan-2-yl)piperidin-4-yl]acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Acetone | HCID 180 | — |
| Reactant | Methyl 4-piperidineacetate | HCID 1515259 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | [1-(Propan-2-yl)piperidin-4-yl]acetic acid | HCID 23062749 | — |
Reaction Steps
Methyl 4-piperidineacetate (0.6 g, 3.82 mmol) was dissolved in methylene chloride (20 mL), acetone (1 mL), acetic acid (0.26 mL) and sodium triacetoxyborohydride (1.21 g, 5.73 mmol) were added, and the mixture was stirred overnight at room temperature. The solvent was evaporated, and work-up according to a conventional method gave a crude product. The obtained crude product was dissolved in 6 N aqueous hydrogen chloride solution, and the mixture was stirred overnight at 80° C. The solvent was evaporated to give the title compound, which was used for the synthesis of A-22.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07879863B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-278b2b9ef82641e8baec3c3413e259c5 |
| Source note | uspto-grants-2011_02 |