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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 56037Generated: October 29, 2026

Benzophenone → N-[(2Z)-2-(3,5-dichloro-2-pyridinyl)-2-[1-(4-fluorophenyl)ethoxyimino]ethyl]-2-(trifluoromethyl)benzamide

https://huagongshe.com/reaction/56037

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzophenoneHCID 3102—
ReactantN-[2-(3,5-dichloropyridin-2-yl)-2-[1-(4-fluorophenyl)ethoxyimino]ethyl]-2-(trifluoromethyl)benzamideHCID 131736904—
SolventAcetonitrileHCID 6342—
ProductN-[(2Z)-2-(3,5-dichloro-2-pyridinyl)-2-[1-(4-fluorophenyl)ethoxyimino]ethyl]-2-(trifluoromethyl)benzamideHCID 11807152557.3%

Reaction Steps

To 171 mg of N-[2-(3,5-dichloropyridin-2-yl)-2-[1-(4-fluorophenyl)ethoxyimino]ethyl]-2-(trifluoromethyl)benzamide in 3 ml of acetonitrile, 1 mg of benzophenone was added, and the mixture was irradiated with light for 12 hours in a quartz cell (manufactured by Fine, 4 clear windows for spectroscopy) using a 100 W high-pressure mercury lamp (manufactured by USHIO INC., lamp: UM-102, power supply: UM-103B-B). After completion of the reaction, the solvent was evaporated under reduced pressure, and the resulting residue was purified by silica gel column chromatography using ethyl acetate-hexane (with a gradient of from 5:95 to 50:50) as the eluent to obtain 98 mg of the desired product as a pale yellow resinous substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434684B2
Source datasetuspto-grants-2016_09
ORD IDord-7cb67c2e360548d7a08ba25402437625
Source noteuspto-grants-2016_09