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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1777027Generated: November 3, 2026

3-Chloro-6-hydroxyacetophenone → N-[(E)-1-(5-chloro-2-hydroxyphenyl)ethylideneamino]-3-(dimethylsulfamoyl)benzamide

https://huagongshe.com/reaction/1777027

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-6-hydroxyacetophenoneHCID 74061—
Reactant3-(Hydrazinecarbonyl)-N,N-dimethylbenzene-1-sulfonamideHCID 3848951—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductN-[(E)-1-(5-chloro-2-hydroxyphenyl)ethylideneamino]-3-(dimethylsulfamoyl)benzamideHCID 13557618718.4%

Reaction Conditions

Temperature120 °C

Reaction Steps

3-(Hydrazinecarbonyl)-N,N-dimethylbenzenesulfonamide (50 mg, 0.0.206 mmol) and 1-(5-chloro-2-hydroxyphenyl)ethanone (35.1 mg, 0.206 mmol) were dissolved in methanol (4 mL) in the presence of acetic acid as a catalyst, and the reaction mixture was heated via microwave irradiation to 120° C. for 30 min. The reaction was monitored by TLC. Upon completion of the reaction and following cooling, the solvent was removed by vacuum, and the resulting crude material was purified by flash column chromatography (2% CH3OH/CH2Cl2) affording the title compound as a solid (15 mg). 1H NMR (400 MHz, acetone-d6): δ 8.29 (m, 2H), 8.01 (d, 1H, J=8.4 Hz), 7.83 (t, 1H, J=8.4 Hz), 7.62 (d, 1H, J=2.4 Hz), 7.32 (dd, 1H, J=2.4 & 8.8 Hz), 6.96 (d, 1H, J=8.8 Hz), 2.73 (s, 6H), 2.58 (s, 3H). ESI-MS: 396.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266838B2
Source datasetuspto-grants-2016_02
ORD IDord-6749450f07b94c4682b9b992ce429772
Source noteuspto-grants-2016_02