Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 431383Generated: October 26, 2026

3-(Trifluoromethyl)aniline → 3,5-Di(benzyloxy)-3'-(trifluoromethyl)benzanilid

https://huagongshe.com/reaction/431383

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)anilineHCID 7375—
Reactant3,5-Bis(benzyloxy)benzoyl chlorideHCID 10831869—
SolventTetrahydrofuranHCID 8028—
Product3,5-Di(benzyloxy)-3'-(trifluoromethyl)benzanilidHCID 10277296—

Reaction Steps

(Examplary Compound 8). The title compound was prepared according to the procedure of Scheme I-A, starting from 3,5-bis(benzyloxy)benzoic acid chloride and 3-(trifluoromethyl)aniline in THF solution. White solid, yield 0.250 g (69%). 1H NMR (DMSO-d6, 400 MHz), δ: 10.47 (s, 1H); 8.24 (s, 1H); 8.06 (d, J=8.3 Hz, 1H); 7.60 (t, J=8.0 Hz, 1H); 7.51-7.32 (m, 11H); 7.25 (s, 2H); 6.95 (s, 1H); 5.18 (s, 4H). Anal: Calcd. for C28H22F3NO3: 70.43; H, 4.64; N, 2.93. Found: C, 70.58; H, 4.67; N, 2.91.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06656971B2
Source datasetuspto-grants-2003_12
ORD IDord-bbea766bfac34e7cb3a7c065633ef599
Source noteuspto-grants-2003_12