HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 877637Generated: October 30, 2026
3-Chloro-6-hydroxyacetophenone → HCID 136374358, compound
https://huagongshe.com/reaction/877637
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Chloro-6-hydroxyacetophenone | HCID 74061 | — |
| Reactant | HCID 71258107 | HCID 71258107 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 136374358 | HCID 136374358 | 21.28% |
Reaction Steps
2-(morpholinosulfonyl)benzohydrazide (30 mg, 0.105 mmol) and 1-(5-chloro-2-hydroxyphenyl)ethanone (17.94 mg, 0.105 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)-2-(morpholinosulfonyl)benzohydrazide (10 mg, 0.022 mmol, 21.28% yield) as a solid. 1H NMR (CD3OD, 400 MHz): δ 7.95 (d, 1H, J=8.0 Hz), 7.95-7.70 (m, 2H), 7.66 (d, 1H, J=7.6 Hz), 7.56 (d, 1H, J=2.8 Hz), 7.25 (dd, 1H, J=2.8 & 8.8 Hz), 6.91 (d, 1H, J=8.4 Hz), 3.66 (m, 4H), 3.2 (m, 4H), 2.36 (s, 3H). Mass [M+H]+:438.1
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08987335B2 |
|---|
| Source dataset | uspto-grants-2015_03 |
|---|
| ORD ID | ord-d8f5084b22ef40dc9290f539cf614d1f |
|---|
| Source note | uspto-grants-2015_03 |
|---|