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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651330Generated: October 31, 2026

Imidazole → (2R)-[t-butyloxycarbonyl(4'-chlorobiphenyl-4-sulfonyl)amino]-4-iodobutyric acid t-butyl ester

https://huagongshe.com/reaction/651330

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantIodineHCID 807—
ReactantTriphenylphosphineHCID 11776—
Reactant(2R)-[t-butoxycarbonyl(4'-chlorobiphenyl-4-sulfonyl)amino]4-hydroxybutyric acid t-butyl esterHCID 69287155—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product(2R)-[t-butyloxycarbonyl(4'-chlorobiphenyl-4-sulfonyl)amino]-4-iodobutyric acid t-butyl esterHCID 5372942378%

Reaction Steps

A solution of the title E compound, (2R)-[t-butoxycarbonyl(4′-chlorobiphenyl-4-sulfonyl)amino]4-hydroxybutyric acid t-butyl ester (2.0 g, 9.58 mmol) in 50 mL dichloromethane is sequentially treated with iodine (2.88 g, 14.37 mmol), triphenylphosphine (3.72 g, 14.37 mmol) and imidazole (0.97 g, 14.37 mmol) at RT. After 2 h, 20 mL of methanol are added and the reaction mixture is stirred at RT for 30 min further. The solvent is evaporated and the product is purified by chomatography on silica gel (eluant; 1/19—EtOAc/hexane) to afford 2.46 g (78%) of (2R)-[t-butyloxycarbonyl(4′-chlorobiphenyl-4-sulfonyl)amino]-4-iodobutyric acid t-butyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06277987B1
Source datasetuspto-grants-2001_08
ORD IDord-ab097ab6517041a2acaf05482c829cc6
Source noteuspto-grants-2001_08