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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815164Generated: October 30, 2026

Triphenylphosphine → HCID 86588701, compound

https://huagongshe.com/reaction/1815164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactanttert-Butyl 2-(hydroxymethyl)pyrrolidine-1-carboxylateHCID 550865—
ReactantDiethyl azodicarboxylateHCID 5462977—
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-hexafluoro-propan-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 DEAD (1.55 mL) slowly. The reaction was stirred at RT for 4 h and at reflux overnight. After filtration to remove solids, the filtrate was concentrated and the residue was taken up into Et2O. The organic phase was washed with saturated NaHCO3 and brine. The organic layer was dried over MgSO4 and evaporated to give a 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 numberUS06878714B2
Source datasetuspto-grants-2005_04
ORD IDord-51a51c604cc24ec3bed77ed885544183
Source noteuspto-grants-2005_04