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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1777029Generated: November 2, 2026

3-Chloro-6-hydroxyacetophenone → HCID 136276620, compound

https://huagongshe.com/reaction/1777029

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-6-hydroxyacetophenoneHCID 74061—
ReactantHCID 86714255HCID 86714255—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 136276620HCID 13627662033.1%

Reaction Conditions

Temperature120 °C

Reaction Steps

5-Bromo-6-chloronicotinohydrazide (15 mg, 0.060 mmol) and 1-(5-chloro-2-hydroxyphenyl)ethanone (10.22 mg, 0.060 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 (8 mg). 1H NMR (400 MHz, DMSO-d6): δ 8.39 (d, 1H, J=2.4 Hz), 8.28 (s, 1H), 7.63 (d, 1H, J=2.4 Hz), 7.32 (dd, 1H, J=2.4 & 8.8 Hz), 7.06 (d, 1H, J=6.8 Hz), 6.92 (d, 1H, J=9.2 Hz), 6.81 (d, 1H, J=6.8 Hz), 2.47 (s, 3H). ESI-MS: 404.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266838B2
Source datasetuspto-grants-2016_02
ORD IDord-e30b8f1847ed43a0b0eeb2b94492b373
Source noteuspto-grants-2016_02