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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836604Generated: October 30, 2026

Hydrochloric Acid → O-(4-fluorophenyl)-L-homoserine ethyl ester hydrochloride

https://huagongshe.com/reaction/1836604

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantN,N,N',N'-TetramethylazodicarboxamideHCID 4278—
Reactant4-FluorophenolHCID 9732—
ReactantTriphenylphosphineHCID 11776—
Reactant(S)-tert-Butyl 2-((tert-butoxycarbonyl)amino)-4-hydroxybutanoateHCID 11054918—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductO-(4-fluorophenyl)-L-homoserine ethyl ester hydrochlorideHCID 68613683—

Reaction Steps

To a solution of BOC-L-homoserine t-butyl ester (3.2 g, 11.6 mmol) in tetrahydrofuran is added triphenylphosphine (7.59 g, 29 mmol), p-fluorophenol (2.08 g, 18.6 mmol) and 1,1′-azobis(N,N-dimethylformamide) (3.2 g, 18.6 mmol). The mixture is stirred overnight, washed with brine, dried over MgSO4, and the solvent is removed to give an orange oil. The oil is purified by flash chromatography (SiO2, 85% hexane/15% ethyl acetate) to give a clear oil which is dissolved in ethanol (100 mL) and the solution is saturated with HCl gas, then stirred overnight. The mixture is concentrated to give O-(4-fluorophenyl)-L-homoserine ethyl ester hydrochloride as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06777443B2
Source datasetuspto-grants-2004_08
ORD IDord-3451224190f243ac99dca055d6cf1663
Source noteuspto-grants-2004_08