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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 913772Generated: October 31, 2026

Diisopropylethylamine → HCID 86620728, compound

https://huagongshe.com/reaction/913772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantPropylphosphonic anhydrideHCID 111923—
Reactant3,3,3-Trifluoropropionic acidHCID 2777972—
ReactantHCID 86620681HCID 86620681—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86620728HCID 8662072870.3%

Reaction Steps

A mixture of {[6-amino-3-cyano-2-(trifluoromethyl)phenyl]methyl}(triphenyl)phosphonium bromide (0.50 g, 0.92 mmol), 3,3,3-trifluoropropanoic acid (0.175 g, 1.40 mmol), 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphorinane 2,4,6-trioxide (2.60 g, 4.10 mmol, 50% in EtOAc) and DIEA (0.65 mL, 3.70 mmol) in THF (25 mL) was stirred at ambient temperature for 6 h. The mixture was concentrated and then diluted with anhydrous DMF (15 mL) and stirred at 100° C. for 18 h. The reaction was poured into water (100 mL) and extracted with Et2O (2×60 mL). The combined organic portions were washed with sat'd NaHCO3 (50 mL) and brine (50 mL). Drying (MgSO4), filtration, and concentration was followed by purification (SiO2, 30% EtOAc in hexanes) to afford 2-(2,2,2-trifluoroethyl)-4-(trifluoromethyl)-1H-indole-5-carbonitrile (0.189 g, 70%) as a pale yellow solid:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026262B2
Source datasetuspto-grants-2011_09
ORD IDord-dd466978d87d417ba16f50d8f8625568
Source noteuspto-grants-2011_09