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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914585Generated: November 3, 2026

(R)-beta-aminophenethyl alcohol → (S)-2-(4-Fluoro-phenyl)-piperidine

https://huagongshe.com/reaction/1914585

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-beta-aminophenethyl alcoholHCID 2724025—
ReactantAC1Ofb5VHCID 7048023—
Product(S)-2-(4-Fluoro-phenyl)-piperidineHCID 7022098—

Reaction Steps

(S)-2-(4-Fluoro-phenyl)-piperidine (0.31 g) was prepared by analogous methods to those used in the preparation of (R)-2-(4-fluoro-phenyl)-piperidine but starting from (R)-(−)-2-phenylglycinol. LCMS m/z 180.12 [M+H]+ R.T.=1.75-2.1 min (Analytical Method 6), which was used in the synthesis of EE-50.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614209B2
Source datasetuspto-grants-2013_12
ORD IDord-ddf513561a8c4b4cba72f955df7fd29e
Source noteuspto-grants-2013_12