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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Chloro-6-hydroxyacetophenone | HCID 74061 | — |
| Reactant | HCID 16412815 | HCID 16412815 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 136641854 | HCID 136641854 | 31.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08987335B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-3501394e2c43408ea23b9d2528a8ecc3 |
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| Source note | uspto-grants-2015_03 |
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