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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839363Generated: November 3, 2026

Aniline → 3,3-Dianilino-1-(2,6-dichloro-5-fluoro-3-pyridinyl)-2-propen-1-one

https://huagongshe.com/reaction/1839363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
Reactant3,3-Dichloro-1-(2,6-dichloro-5-fluoro-3-pyridinyl)-2-propen-1-oneHCID 21948132—
Solvent1,4-DioxaneHCID 31275—
Product3,3-Dianilino-1-(2,6-dichloro-5-fluoro-3-pyridinyl)-2-propen-1-oneHCID 2194813849%

Reaction Steps

To a 0° C. solution of 3,3-dichloro-1-(2,6-dichloro-5-fluoro-3-pyridinyl)-2-propen-1-one (6.70 g, 23.2 mmol) in dioxane (50 mL) was added TEA (9.7 mL, 69.6) followed by aniline (6.3 mL, 69.6 mmol). After 1 h the reaction was allowed to warm to room temperature and was stirred overnight. The mixture was concentrated in vacuo until most of the solvent was removed and then the residue was diluted with water and extracted with CH2Cl2 (2×). The combined organic extracts were washed with water, dried over Na2SO4 and concentrated in vacuo. Purification of the residue by silica gel Biotage chromatography provided 3,3-dianilino-1-(2,6-dichloro-5-fluoro-3-pyridinyl)-2-propen-1-one as yellow solid (4.2 g, 49%): LCMS RT: 3.47 min; MH+: 402.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677352B1
Source datasetuspto-grants-2004_01
ORD IDord-7bad4197d3134a5ab6c45d18d73b3cf3
Source noteuspto-grants-2004_01