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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276732Generated: October 25, 2026

Imidazole → N-Boc-5-Iodo-L-norvaline tert-butyl ester

https://huagongshe.com/reaction/276732

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantIodineHCID 807—
ReactantTriphenylphosphineHCID 11776—
Reactant(S)-tert-butyl 2-((tert-butoxycarbonyl)amino)-5-hydroxypentanoateHCID 10062769—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductN-Boc-5-Iodo-L-norvaline tert-butyl esterHCID 15479354—

Reaction Steps

To a solution of t-butyl (S)-5-hydroxy-2-(t-butoxycarbonylamino)-pentanoate (5.79 g, 20.0 mmol), triphenylphosphine (8.13 g, 31.0 mmol) and imidazole (2.04 g, 30.0 mmol) in CH2Cl2 (200 mL) at room temperature is added iodine (6.35 g, 25.0 mmol), portionwise, over 30 minutes. The mixture is then stirred 16 hours at room temperature. Methanol (20 mL) is added to the solution, which is then stirred an additional 1 hour. Solvent is evaporated, and the residue is purified by chromatography (silica, 33% EtOAc/hexane) to yield t-butyl (S)-5-iodo-2-(t-butoxycarbonylamino)-pentanoate as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06353017B1
Source datasetuspto-grants-2002_03
ORD IDord-7c6289faa39441d3824ed62cc75a584e
Source noteuspto-grants-2002_03