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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911505Generated: November 4, 2026

(S)-2,2-dimethyl-4-((E)-2-phenyl-propenyl)-oxazolidine-3-carboxylic acid tert-butyl ester → (S)-2-amino-4-phenyl-pentan-1-ol

https://huagongshe.com/reaction/1911505

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-2,2-dimethyl-4-((E)-2-phenyl-propenyl)-oxazolidine-3-carboxylic acid tert-butyl esterHCID 68710162—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventChloroformHCID 6212—
Product(S)-2-amino-4-phenyl-pentan-1-olHCID 6870971886.5%

Reaction Steps

A solution of (S)-2,2-dimethyl-4-((E)-2-phenyl-propenyl)-oxazolidine-3-carboxylic acid tert-butyl ester (700 mg) in EtOH (30 ml) and CHCl3 (15 ml) was treated with 10% Pd/C (200 mg) and hydrogenated with a balloon overnight. The catalyst was filtered off, washed with EtOH and concentrated. The residue was dissolved in EtOH (10 ml) and treated with 2N HCl (15 ml). The mixture was heated for 90 min to 100° C., then concentrated. The residue was taken up in 1N NaOH and extracted with CH2Cl2/MeOH 4:1. The organic layer was dried over MgSO4, filtrated and concentrated. The crude product was purified by column chromatography (SiO2; gradient: CH2Cl2->CH2Cl2/MeOH 9:1) to give (S)-2-amino-4-phenyl-pentan-1-ol (342 mg) as off-white waxy solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604061B2
Source datasetuspto-grants-2013_12
ORD IDord-9f813112bb934ecb833b4a889f1be558
Source noteuspto-grants-2013_12