Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587188Generated: October 29, 2026

Triphenyl phosphite → 2,2,2-Trifluoro-1-[3-(trifluoromethyl)phenyl]ethan-1-ol

https://huagongshe.com/reaction/587188

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenyl phosphiteHCID 7540—
ReactantN-bromobutanimideHCID 67184—
Reactant1-(3,5-Dichlorophenyl)-2,2,2-trifluoroethanolHCID 61644685—
Reactant1-(1-Bromo-2,2,2-trifluoroethyl)-3,5-dichlorobenzeneHCID 86675118—
SolventDichloromethaneHCID 6344—
Product2,2,2-Trifluoro-1-[3-(trifluoromethyl)phenyl]ethan-1-olHCID 24455940%

Reaction Conditions

Temperature25 °C

Reaction Steps

1-(1-Bromo-2,2,2-trifluoroethyl)-3,5-dichlorobenzene (AI1). To a stirred solution of 1-(3,5-dichlorophenyl)-2,2,2-trifluoroethanol (4.0 g, 16.3 mmol) in CH2Cl2 (50 mL), were added NBS (2.9 g, 16.3 mmol) and triphenyl phosphite (5.06 g, 16.3 mmol), and the resultant reaction mixture was heated at reflux for 18 h. After the reaction was deemed complete by TLC, the reaction mixture was cooled to 25° C. and was concentrated under reduced pressure. Purification by flash column chromatography (SiO2, 100-200 mesh; eluting with 100% pentane) afforded the title compound as a liquid (2.0 g, 40%): 1H NMR (400 MHz, CDCl3) δ 7.41 (s, 3H), 5.00 (m, 1H); EIMS m/z 306 ([M]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09226500B2
Source datasetuspto-grants-2016_01
ORD IDord-615497d5e4d14abe91fd9b0f707625a6
Source noteuspto-grants-2016_01