Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1840288Generated: October 27, 2026

5-Fluoro-2-(2,2,2-trifluoroethoxy)nitrobenzene → 5-Fluoro-2-(2,2,2-trifluoroethoxy)aniline

https://huagongshe.com/reaction/1840288

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Fluoro-2-(2,2,2-trifluoroethoxy)nitrobenzeneHCID 23447921—
CatalystNickelHCID 935—
SolventEthyl AcetateHCID 8857—
Product5-Fluoro-2-(2,2,2-trifluoroethoxy)anilineHCID 1748541390.6%

Reaction Conditions

Temperature22.5 °C

Reaction Steps

A mixture of 0.66 g of Compound 5A and 0.07 g of Raney-Nickel in 20 mL of ethyl acetate was stirred for 14 hours at 20-25° C. The organic layer was separated and the mixture extracted with 2×40 mL of ethyl acetate. The combined organic layers were washed with 20 mL of brine, dried over sodium sulphate and evaporated to dryness in vacuo to afford 0.52 g (90.6%) of Compound 5B as an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06680319B2
Source datasetuspto-grants-2004_01
ORD IDord-9ddd484ec198457f9944e37de7f65efa
Source noteuspto-grants-2004_01