HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095273Generated: October 25, 2026
3,4,5-Trimethoxyphenol → 2'-Hydroxy-4',5',6'-trimethoxy-4-nitrochalcone
https://huagongshe.com/reaction/1095273
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3,4,5-Trimethoxyphenol | HCID 69505 | — |
| Reactant | 3-(4-nitrophenyl)prop-2-enoyl Chloride | HCID 319463 | — |
| Product | 2'-Hydroxy-4',5',6'-trimethoxy-4-nitrochalcone | HCID 72767069 | 22% |
Reaction Steps
A mixture of 3,4,5-trimethoxyphenol (1.85 g, 10 mmol) and 4-nitrocinnamoyl chloride (2.11 g, 10 mmol) was dissolved in BF3-Et2O complex (10 ml) and heated to 80° C. for 10 min, and then quenched with excess of water. The aqueous layer was extracted with dichloromethane. The combined organic layer was concentrated and the residue was purified by column chromatography on silica gel (CH2Cl2:EtOAc:Hexane=1:1:3) gave 7a (0.79 g, 22%) and 7b (1.54 g, 43%). 1H NMR (400 MHz, CDCl3) μ 3.81 (s, 3H), 3.90 (s, 3H), 3.91 (s, 3H), 6.29 (s, 1H), 7.74 (d, J=8.8 Hz, 2H), 7.76 (d, J=16.0 Hz, 1H), 8.01 (d, J=16.0 Hz, 1H), 8.26 (d, J=8.8 Hz, 2H), 13.44 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08138165B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-4049c48a3e50449dade86f120b203cfc |
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| Source note | uspto-grants-2012_03 |
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