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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2211638Generated: November 1, 2026

Triphenylphosphine → HCID 86588701, compound

https://huagongshe.com/reaction/2211638

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactanttert-Butyl 2-(hydroxymethyl)pyrrolidine-1-carboxylateHCID 550865—
Reactant2-(3-Aminophenyl)-1,1,1,3,3,3-hexafluoropropan-2-olHCID 13320609—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86588701HCID 86588701—

Reaction Steps

To a mixture of 2-(3-amino-phenyl)-1,1,1,3,3,3-hexafluoropropan-2-ol (1.30 g), 2-hydroxymethyl-pyrrolidine-1-carboxylic acid tert-butyl ester (1.04 g), PPh3 (2.64 g) and molecular sieves 4 Å in THF (100 mL) was added diethyl diazocarboxylate (1.55 mL) slowly. The reaction was stirred at RT for 4 h and at reflux for overnight. After filtration to remove solids, the filtrate was concentrated and the residue was taken into Et2O. The organic phase was washed with saturated NaHCO3 and brine. The organic layer was dried over MgSO4 and evaporated to give a crude compound as very viscous brown oil, which was purified by chromatography through silica gel (500 g, 30% to 50% EtOAc in hexanes) to afford 2-[1-(3-amino-phenyl)-2,2,2-trifluoro-1-trifluoromethyl-ethoxymethyl]-pyrrolidine-1-carboxylic acid tert-butyl ester as a light brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101868B2
Source datasetuspto-grants-2006_09
ORD IDord-820588b3c1074260bc4526c5ba5c864f
Source noteuspto-grants-2006_09