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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 658229Generated: October 29, 2026

HCID 131729327, compound → HCID 67533258, compound

https://huagongshe.com/reaction/658229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 131729327HCID 131729327—
SolventEthanolHCID 702—
ProductHCID 67533258HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08076359B2
Source datasetuspto-grants-2011_12
ORD IDord-ce2ff6d424ba4d7e85c9f42956f39446
Source noteuspto-grants-2011_12