HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → Tert-butyl (R)-2-phenyl-2-(piperidin-1-YL)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Glutaraldehyde | HCID 3485 | — |
| Reactant | Cyano-borohydride | HCID 498716 | — |
| Reactant | H-D-Phg-otbu hcl | HCID 56777188 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tert-butyl (R)-2-phenyl-2-(piperidin-1-YL)acetate | HCID 59166413 | — |
Reaction Steps
To a slurry of (R)-tert-butyl 2-amino-2-phenylacetate HCL (Chem-Impex, 0.200 g, 0.821 mmol), MP-cyanoborohydride (2.44 mmol/g; 500 mg) and acetic acid (0.141 mL, 2.462 mmol) in MeOH (2.00 mL) and CH2Cl2 (2 mL) at rt was added glutaraldehyde (0.155 mL, 0.821 mmol) as a 50% solution in water. The reaction was stirred for 30 min., the reaction filtered, washed with MeOH and concentrated. The residue was taken up in CH2Cl2, washed with saturated NaHCO3, dried (Na2SO4) and concentrated to give the title compound. MS (DCI; M+H) m/z=276.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09278922B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-57f9213d03974fb2ba99a31cc001e0b6 |
| Source note | uspto-grants-2016_03 |