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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252294Generated: October 27, 2026

3-(Trifluoromethyl)aniline → 1-(3-Thienyl)-3-{[3-(trifluoromethyl)phenyl]imino}-1,3-dihydro-2H-indol-2-one

https://huagongshe.com/reaction/252294

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)anilineHCID 7375—
Reactant1-(3-Thienyl)-1H-indole-2,3-dioneHCID 22022431—
Product1-(3-Thienyl)-3-{[3-(trifluoromethyl)phenyl]imino}-1,3-dihydro-2H-indol-2-oneHCID 2202244722%

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of 1-(3-thienyl)-2H-indole-2,3-dione (25 mg, 0.11 mmol) (prepared as described below) and 3-trifluoromethylaniline (14 uL, 0.11 mmol) was heated neat at 140° C. for 2 h. The crude material was purified by preparative TLC using a mixture of 3:7 ethyl acetate and hexane as the eluent, giving the desired product as a yellow solid (7.3 mg, 0.02 mmol, 22%). 1H NMR (400 MHz) δ 7.62-7.19 (m, 9H), 6.94 (d, J=8.0, 1H), 6.76 (t, J=7.6, 1H); ESI-MS m/z found 373 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868034B2
Source datasetuspto-grants-2011_01
ORD IDord-32508782d37148c88830af0caf086797
Source noteuspto-grants-2011_01