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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28614Generated: October 25, 2026

Methyl 4-nitrobenzoate → 1-(4-Nitrophenyl)-2,2,2-trifluoroethane-1,1-diol

https://huagongshe.com/reaction/28614

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-nitrobenzoateHCID 12083—
Reactant(Trifluoromethyl)trimethylsilaneHCID 552549—
ReactantTetrabutylammonium FluorideHCID 2724141—
SolventDichloromethaneHCID 6344—
Product1-(4-Nitrophenyl)-2,2,2-trifluoroethane-1,1-diolHCID 6898756747%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a mixture of 4-nitro-benzoic acid methyl ester (1.8 g, 9.9 mmol), trimethyl-trifluoromethyl-silane (2.0 ml, 12.8 mmol) and anhydrous dichloromethane (20 ml), cooled at −78° C., was added a solution of tetrabutylammonium fluoride in dichloromethane (1 M, 0.5 ml) previously dried over 4A molecular sieves. After stirring for 72 hours, hydrochloric acid (1 M, 50 ml) was added. The mixture was treated with saturated aqueous sodium chloride solution (100 ml) and extracted with ethyl acetate (100 ml). The organic extract was concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel eluting with ethyl acetate-hexane (1:3) providing 2,2,2-trifluoro-1-(4-nitro-phenyl)-ethane-1,1-diol (1.1 g, 47% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07419984B2
Source datasetuspto-grants-2008_09
ORD IDord-22b8025c6fed4512a99f7b5726576bc2
Source noteuspto-grants-2008_09