HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 131729327, compound → HCID 67533258, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 131729327 | HCID 131729327 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 67533258 | HCID 67533258 | — |
Reaction Steps
Racemic trans-1-tert-butyl 3-ethyl 4-{4-[2-(2,6-dichloro-4-methylphenoxy)-ethoxy]phenyl}-piperidine-1,3-dicarboxylate was resolved by a Chiral Pak AD preparative column (15% EtOH in Hex) to afford two enantiomers. 1-tert-Butyl 3-ethyl (3R,4S)-4-{4-[2-(2,6-dichloro-4-methylphenoxy)ethoxy]-phenyl}piperidine-1,3-dicarboxylate was eluted as the slower enantiomer (retention time=26.5 min).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08076359B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-ce2ff6d424ba4d7e85c9f42956f39446 |
| Source note | uspto-grants-2011_12 |