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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063523Generated: November 1, 2026

Aniline → 3,3-Dianilino-1-[2,6-dichloro-4-(trifluoromethyl)-3-pyridinyl]-2-propen-1-one

https://huagongshe.com/reaction/1063523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
Reactant3,3-Dichloro-1-[2,6-dichloro-4-(trifluoromethyl)-3-pyridinyl]-2-propen-1-oneHCID 21948141—
Solvent1,4-DioxaneHCID 31275—
Product3,3-Dianilino-1-[2,6-dichloro-4-(trifluoromethyl)-3-pyridinyl]-2-propen-1-oneHCID 2194818443%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of aniline (18.4 mL, 202 mmol) in TEA (28.2 mL, 202 mmol) was added slowly to a cooled (0° C.) and stirred solution of 3,3-dichloro-1-[2,6-dichloro-4-(trifluoromethyl)-3-pyridinyl]-2-propen-1-one (22.9 g, 67.4 mmol) in dioxane (220 mL). The reaction was allowed to warm to room temperature and was stirred overnight. The mixture was treated with 10% HCI and extracted with Et2O (3×). The combined organic extracts were washed with brine, dried over Na2SO4 and concentrate in vacuo. Silica gel flash chromatography of the residue using 6:1 Hex:EtOAc gave 3,3-dianilino-1-[2,6 dichloro-4-(trifluoromethyl)-3-pyridinyl]-2-propen-1-one as an off-white solid (13.10 g, 43%): 1H-NMR (d6-DMSO, 300 MHz) δ12.24 (br s, 1H), 9.20 (br s, 1H), 7.95 (s, 1H), 7.12-7.42 (m, 1H), 4.82 (s, 1H); Rf=0.60 (6:1 Hex:EtOAc).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06964971B2
Source datasetuspto-grants-2005_11
ORD IDord-0bd35b1bebb643309164014e2ea839b3
Source noteuspto-grants-2005_11