Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 877614Generated: October 31, 2026

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

https://huagongshe.com/reaction/877614

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 numberUS08987335B2
Source datasetuspto-grants-2015_03
ORD IDord-b47d5b2afde643f3a1d5d03574a94d9c
Source noteuspto-grants-2015_03