Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281281Generated: November 2, 2026

Acetonitrile → HCID 23506040, compound

https://huagongshe.com/reaction/1281281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
Reactant2-(Trifluoromethyl)oxiraneHCID 520769—
ReactantYtterbium triflateHCID 2733225—
ReactantHCID 131723493HCID 131723493—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
ProductHCID 23506040HCID 23506040—

Reaction Steps

To a CH3CN (2 mL) solution of amine (0.20 g, 0.58 mmol) from EX-601B was added 1,1,1-trifluoro-2,3-epoxypropane (0.10 mL, 1.2 mmol) and Yb(OTf)3 (0.035 g, 0.056 mmol). The cloudy solution was stiffed in a sealed flask at 40° C. After 18 h, additional 1,1,1-trifluoro-2,3-epoxypropane (0.20 mL, 2.4 mmol) and Yb(OTf)3 (0.035 g, 0.056 mmol) were added, and the mixture was heated an additional 4 h. diluted with diethyl ether and washed with water and brine. The organic layer was dried (MgSO4) and evaporated to an oil. Purification by flash chromatography on silica gel eluting with 10% ethyl acetate in hexane gave an oil which was dissolved in EtOH, stripped and dried in vacuo to give 0.14 g (53%) of the desired 3[(3-phenoxyphenyl) [[(3-(3-furanyl)phenyl]methyl]amino]-1,1,1-trifluoro-2-propanol product as a colorless oil, >99% pure by HPLC analysis. Anal. calcd. for C26H22NO3F3.0.3 EtOH:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451823B1
Source datasetuspto-grants-2002_09
ORD IDord-4afc46a24bbc42eb82f3b55b70f476f4
Source noteuspto-grants-2002_09