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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1777062Generated: November 3, 2026

3-Chloro-6-hydroxyacetophenone → HCID 136265205, compound

https://huagongshe.com/reaction/1777062

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-6-hydroxyacetophenoneHCID 74061—
ReactantHCID 71258151HCID 71258151—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 136265205HCID 13626520540.5%

Reaction Conditions

Temperature120 °C

Reaction Steps

3-(hydrazinecarbonyl)benzenesulfonamide (50 mg, 0.232 mmol) and 1-(5-chloro-2-hydroxyphenyl)ethanone (39.6 mg, 0.232 mmol) was dissolved in methanol (Volume: 4 ml) in the presence of acetic acid as a catalyst and then the reaction mixture was heated via microwave irradiation to 120° C. for 30 min. Reaction was monitored by TLC. After completion of the reaction, following cooling, the solvent was removed by vacuum and the resulting crude material was purified by flash column chromatography (2% CH3OH/CH2Cl2) afforded the product (E)-3-(2-(1-(5-chloro-2-hydroxyphenyl)ethylidene)hydrazinecarbonyl)benzenesulfonamide (36 mg, 0.094 mmol, 40.4% yield) as a solid. 1H NMR (DMSO-d6, 400 MHz): δ 8.34 (s, 1H), 8.15 (d, 1H, J=7.6 Hz), 8.02 (d, 1H, J=7.6 Hz), 7.73 (t, 1H, J=8.0 Hz), 7.64 (m, 1H), 7.51 (bs, 2H), 7.32 (dd, 1H, J=2.4 & 8.4 Hz), 6.92 (d, 1H, J=8.4 Hz), 2.49 (s, 3H). Mass [M+H]+: 368.0

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266838B2
Source datasetuspto-grants-2016_02
ORD IDord-df6d2729e4a44a178a37e1068e716078
Source noteuspto-grants-2016_02