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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 634944Generated: October 31, 2026

Sodium Iodide → N-[(carbobenzyloxycarbonyl)valinyl]-3-amino-4-oxo-5-(2,3,5,6-tetrafluorophenyloxy)-pentanoic acid, tert-butyl ester

https://huagongshe.com/reaction/634944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium 2,3,5,6-tetrafluorophenolateHCID 4611022—
ReactantN-[(carbobenzyloxycarbonyl)valinyl]-3-amino-5-bromo-4-oxo-pentanoic acid, tert-butyl esterHCID 86584480—
SolventAcetoneHCID 180—
SolventEthyl AcetateHCID 8857—
ProductN-[(carbobenzyloxycarbonyl)valinyl]-3-amino-4-oxo-5-(2,3,5,6-tetrafluorophenyloxy)-pentanoic acid, tert-butyl esterHCID 8658447989.7%

Reaction Steps

To a solution of N-[(carbobenzyloxycarbonyl)valinyl]-3-amino-5-bromo-4-oxo-pentanoic acid, tert-butyl ester (3.36 g, 6.73 mmol) in acetone (20 ml) was added dry NaI (0.20 g, 1.35 mmol) and potassium (2,3,5,6-tetrafluoro)-phenoxide (1.37 g, 6.73 mmol) at room temperature and stirred for 1 hour. The reaction mixture was diluted with EtOAc, washed with brine, dried over Na2SO4, filtered and concentrated. The resultant solid was triturated with ether to provide the titled product as a white solid (3.53 g, 6.04 mmol, 89%). MS C28 H32N2O7, [M+Na]+ =607, [M−H]− =583.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06184244B2
Source datasetuspto-grants-2001_02
ORD IDord-530de51681214dd382ead3a581c4fec7
Source noteuspto-grants-2001_02