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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786369Generated: November 2, 2026

Triphenylphosphine → HCID 86588701, compound

https://huagongshe.com/reaction/1786369

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 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 numberUS07507748B2
Source datasetuspto-grants-2009_03
ORD IDord-fa0bf815759d4bbb9e78033bfb630276
Source noteuspto-grants-2009_03