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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839367Generated: October 30, 2026

Aniline → HCID 21948204, compound

https://huagongshe.com/reaction/1839367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantHCID 21948210HCID 21948210—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 21948204HCID 2194820449%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of aniline (1.01 mL, 11.1 mmol) in TEA (1.55 mL, 11.1 mmol) was added slowly to a cooled (0° C.) and stirred solution of 3,3-dichloro-l -(2,6-dichloro-3-pyridinyl)-2-propen-1-one (1.0 g, 3.69 mmol) in dioxane (20 mL). 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. The residue was diluted with water and extracted with EtOAc (3×). The combined organic extracts were washed with water, dried over Na2SO4 and concentrated in vacuo. Silica gel flash chromatography of the residue using 6:1 EtOAc:Hex gave 3,3-dianilino-1-(2,6-dichloro-3-pyridinyl)-2-propen-1-one as pale yellow solid (0.69 g, 49%): LCMS RT: 3.81 min; MH+: 384.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677352B1
Source datasetuspto-grants-2004_01
ORD IDord-17a2ae482c7f4621b2b819a6605f1ad6
Source noteuspto-grants-2004_01