Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2402222Generated: October 25, 2026

4-Fluoro-3-(trifluoromethyl)aniline → HCID 178495898, compound

https://huagongshe.com/reaction/2402222

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluoro-3-(trifluoromethyl)anilineHCID 75377—
ReactantN-Hydroxy-4-[(2-methoxyethyl)amino]-1,2,5-oxadiazole-3-carboximidoyl chlorideHCID 136330165—
ProductHCID 178495898HCID 178495898—

Reaction Steps

The desired compound was prepared according to the procedure of Example 13, step A, using N-hydroxy-4-[(2-methoxyethyl)amino]-1,2,5-oxadiazole-3-carboximidoyl chloride [made according to Example 1, steps A through E] and 3-trifluoromethyl-4-fluoroaniline [Aldrich, product #217778] as the starting materials in quantitative yield. LCMS for C13H14F4N5O3 (M+H)+: m/z=364.0. 1H NMR (400 MHz, CD3OD): δ 7.15 (m, 2H), 7.08 (m, 1H), 3.60 (t, J=5.3 Hz, 2H), 3.46 (t, J=5.3 Hz, 2H), 3.38 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796319B2
Source datasetuspto-grants-2014_08
ORD IDord-07168fd5deb945028bfab441c97562d4
Source noteuspto-grants-2014_08