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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 877642Generated: October 28, 2026

3-Chloro-6-hydroxyacetophenone → HCID 136641854, compound

https://huagongshe.com/reaction/877642

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-6-hydroxyacetophenoneHCID 74061—
ReactantHCID 16412815HCID 16412815—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 136641854HCID 13664185431.5%

Reaction Conditions

Temperature120 °C

Reaction Steps

3-(1,1-dioxidothiomorpholino)benzohydrazide (30 mg, 0.111 mmol) and 1-(5-chloro-2-hydroxyphenyl)ethanone (19.00 mg, 0.111 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 title compound (E)-N′-(1-(5-chloro-2-hydroxyphenyl)ethylidene)-3-(1,1-dioxidothiomorpholino)benzohydrazide (15 mg, 0.035 mmol, 31.3% yield) as a solid. 1H NMR (DMSO-d6, 400 MHz): δ 7.65 (d, 1H, J=2.0 Hz), 7.47 (m, 1H), 7.41 (t, 1H, J=7.6 Hz), 7.36-7.27 (m, 3H), 6.94 (d, 1H, J=8.8 Hz), 3.87 (m, 4H), 3.17 (m, 4H), 2.48 (s, 3H). Mass [M+H]+:422.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987335B2
Source datasetuspto-grants-2015_03
ORD IDord-3501394e2c43408ea23b9d2528a8ecc3
Source noteuspto-grants-2015_03