HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815159Generated: October 29, 2026
Triphenylphosphine → HCID 86588701, compound
https://huagongshe.com/reaction/1815159
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | tert-Butyl 2-(hydroxymethyl)pyrrolidine-1-carboxylate | HCID 550865 | — |
| Reactant | 2-(3-Aminophenyl)-1,1,1,3,3,3-hexafluoropropan-2-ol | HCID 13320609 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86588701 | HCID 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 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06878714B2 |
|---|
| Source dataset | uspto-grants-2005_04 |
|---|
| ORD ID | ord-e7cb34b9957b4b0398bb50a33719d8ef |
|---|
| Source note | uspto-grants-2005_04 |
|---|