Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 634935Generated: October 25, 2026

2,3,5,6-Tetrafluorophenol → tert-Butyl pentanoate

https://huagongshe.com/reaction/634935

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3,5,6-TetrafluorophenolHCID 69858—
ReactantPotassium FluorideHCID 522689—
ReactantN-[(1-methyl-3-isobutyl-indole-2-cabonyl)valinyl]-3-amino-5-bromo-4-oxo-pentanoic acid, tert-butyl esterHCID 86756359—
SolventDimethylformamideHCID 6228—
Producttert-Butyl pentanoateHCID 520048371.5%
ProductN-[(1-methyl-3-isobutyl-indole-2-cabonyl)valinyl]-3-amino-4-oxo-5-(2,3,5,6-tetrafluorophenyloxy)-pentanoic acid, tert-butyl EsterHCID 86756358—

Reaction Steps

Potassium fluoride (21.6 mg, 0.37 mmol) was added to a solution of N-[(1-methyl-3-isobutyl-indole-2-carbonyl)valinyl]-3-amino-5-bromo-4-oxo-pentanoic acid, tert-butyl ester (86.1 mg, 0.149 mmol) and 2,3,5, 6-tetrafluorophenol (27.0 mg, 0.163 mmol) in DMF (2.0 ml). After stirring at room temperature for 3 hours, the reaction mixture was partitioned between ethyl acetate and water. The aqueous layer was back-extracted with ethyl acetate. The organic layers were combined, washed with saturated NaHCO3 solution, and brine, dried over sodium sulfate, and concentrated. The residue was triturated with ether to give the titled product, N-(1-methyl-3-isobutyl-indole-2-carbonyl)-valinyl-3-amino-4-oxo-5-(2,3,5,6-tetral]uorophenyloxy)-pentanoic acid, tert-butyl ester as a white solid (43.8 mg, 44%). TLC (hexane/EtOAc, 50/50): Rf=0.50.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06184244B2
Source datasetuspto-grants-2001_02
ORD IDord-6da38b4177ff47fe80c51126986009bb
Source noteuspto-grants-2001_02