1,1,1-Trifluoro-2-octyl p-nitrobenzoate → 1,1,1-Trifluoro-2-octyl p-aminobenzoate

Participants

Reaction Steps

The reaction liquid was poured into water, and extracted with methylene chloride, then, the organic layer was washed with a diluted hydrochloric acid and water in this order. The organic layer thus recovered was distilled under a reduced pressure to remove the solvent, and subjected to purification by a silica gel chromatography (n-hexane:ethyl acetate=10:2) to obtain 1.9 g of 1,1,1-trifluoro-2-octyl p-nitrobenzoate. The ester was dissolved in 30 ml of ethanol, to which 0.19 g of 5 % Pd-C catalyst was added. After the solution was stirred overnight under hydrogen atmosphere, the Pd-C catalyst was separated by filtration, and then the ethanol was distilled off under a reduced pressure to obtain 1.8 g of 1,1,1-trifluoro-2-octyl p-aminobenzoate which was the desired compound of the reaction [1].

Provenance & Evidence